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Read More Prior Announcements On October 27, 2015, Amsel Medical Corporation announced Filing of 2nd 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device. On February 2, 2015, Amsel Medical Corporation announced Clearance of a 510(k) Pre-Marketing Notification by the US Food and Drug Administration for the Amsel Occluder Device. On July 25, 2014, Amsel Medical Corporation and the Mayo Clinic Announced Signing of a Patent License Agreement. On May 20, 2014, Amsel Medical Corporation announced Filing of a 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device. interview skills en francais About the Amsel Occluder Device The Amsel Occluder Device is designed to easily and securely close blood vessels (veins or arteries as well as hollow ducts) during surgical procedures. The cleared indications for use is: The Amsel Occluder Device is intended for use in open no data general surgery procedures on tubular structures or blood vessels (arteries and veins) wherever a metal ligating clip is indicated and within the size range of 2.0mm to 7.0mm diameter. The currently cleared Amsel Occluder Device employs a proprietary mechanical design that enables a vessel clamp to be introduced during open surgery. The current 510(k) is to add the percutaneous route of administration to the products labeling. The Amsel Occluder Device transfixes the target vessel with the clamp to provide closure. About Amsel Medical Corporation Amsel Medical Corporation, a development stage medical device company, founded in 2011, is developing The Amsel Occluder Device. The company has operations in Cambridge, MA, and Tel Aviv, Israel. The Amsel Occluder Device addresses an estimated 31 million10,11 annual US surgical procedures where vessel closure is required.
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