{"id":72461,"date":"2013-02-13T11:50:52","date_gmt":"2013-02-13T16:50:52","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/freedom-meditech-receives-fda-510k-clearance-for-clearpath-ds-120.php"},"modified":"2013-02-13T11:50:52","modified_gmt":"2013-02-13T16:50:52","slug":"freedom-meditech-receives-fda-510k-clearance-for-clearpath-ds-120","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/freedom\/freedom-meditech-receives-fda-510k-clearance-for-clearpath-ds-120.php","title":{"rendered":"Freedom Meditech Receives FDA 510(k) Clearance for ClearPath DS-120\u2122"},"content":{"rendered":"<p><p>    SAN DIEGO--(BUSINESS WIRE)--  <\/p>\n<p>    Freedom Meditech, Inc., developer of non-invasive ophthalmic    products for the detection of disease and management of patient    health, today announced it has received 510(k) clearance from    the U.S. Food and Drug Administration (FDA) to market and sell    its first product, the ClearPath DS-120 Lens Fluorescence    Biomicroscope.  <\/p>\n<p>    The ClearPath is cleared by FDA as a tool for the measurement    of autofluorescence by scanning the crystalline lens of the eye    with a blue light. In independent scientific studies published    in peer-reviewed journals, elevated autofluorescence    measurements have been linked to high levels of advanced    glycosylated end products which accumulate as a result of the    aging process and the presence of systemic disease.  <\/p>\n<p>    The ClearPath scan is pain free, takes just six seconds and    produces an immediate, quantitative result available to the    patent and healthcare provider. Unlike some eye exams, the scan    does not require dilation or other special preparation by the    patient. The ClearPath is also different from diagnostic tests    in that it is completely non-invasive and does not require a    blood draw to produce a result.  <\/p>\n<p>    Receiving FDA clearance for the ClearPath is the most    significant milestone to date for the company and removes the    last significant risk in product development prior to    marketing, said Craig Misrach, Chairman and CEO of Freedom    Meditech. We are in the process of conducting additional    validation studies which we anticipate will support enhanced    claims in the labeling for the ClearPath including its ability    to further improve patient outcomes and maximize overall public    health.  <\/p>\n<p>    The company plans to launch the ClearPath in the U.S. by the    end of the second quarter 2013. Also, the company is in the    process of acquiring the CE Mark for the product. The CE Mark    is required to sell in the 27 countries that comprise the    European Union and is a gateway to other non-regulated markets.  <\/p>\n<p>    In clinical trial results submitted to the FDA the ClearPath    proved to be more precise than standard of care ophthalmic    devices marketed and widely utilized by health care providers    in the U.S. today. The ClearPath demonstrated a Repeatability    Coefficient of Variation (variability among measurements taken    on the same eye using the same operator and device) and    Reproducibility Coefficient of Variation (variability among    measurements taken on the same eye using different operators    and devices) of 5.8 % and 6.4% respectively.  <\/p>\n<p>    The ClearPath is the first product from Freedom Meditech. Also    in development is the I-SugarX non-invasive monitor that    measures glucose levels in the aqueous of the eye. The I-SugarX    is designed to be operated by holding the small handheld    device, similar to a miniature telescope, in front of the eye    to provide people with diabetes a convenient and pain-free    alternative to the finger stick method of glucose monitoring.  <\/p>\n<p>    About Freedom Meditech Freedom Meditech, Inc. is a    medical device company focused on the commercialization of    novel ophthalmic technologies for the detection of disease and    management of patient health. The company maintains corporate    and engineering operations in San Diego, CA with supporting    research and development activities throughout the state of    Ohio. For more information, visit     <a href=\"http:\/\/www.freedom-meditech.com\" rel=\"nofollow\">http:\/\/www.freedom-meditech.com<\/a>.  <\/p>\n<p>    The I-SugarX is an investigational device and is limited by    federal law to investigational use.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read the original post:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/finance.yahoo.com\/news\/freedom-meditech-receives-fda-510-160000912.html;_ylt=A2KLOzFNxBtRpnYAzOn_wgt.\" title=\"Freedom Meditech Receives FDA 510(k) Clearance for ClearPath DS-120\u2122\">Freedom Meditech Receives FDA 510(k) Clearance for ClearPath DS-120\u2122<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> SAN DIEGO--(BUSINESS WIRE)-- Freedom Meditech, Inc., developer of non-invasive ophthalmic products for the detection of disease and management of patient health, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market and sell its first product, the ClearPath DS-120 Lens Fluorescence Biomicroscope. The ClearPath is cleared by FDA as a tool for the measurement of autofluorescence by scanning the crystalline lens of the eye with a blue light <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/freedom\/freedom-meditech-receives-fda-510k-clearance-for-clearpath-ds-120.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[30],"tags":[],"class_list":["post-72461","post","type-post","status-publish","format-standard","hentry","category-freedom"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/72461"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=72461"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/72461\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=72461"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=72461"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=72461"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}