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FDA Device Clearances: Genetic Test for Breast Cancer, Cervical Disc Replacement Device, Digital Cys
Link ID 2565
Title FDA Device Clearances: Genetic Test for Breast Cancer, Cervical Disc Replacement Device, Digital Cys
Url http://www.medscape.com/viewarticle/569060?src=rss
Description The FDA has approved a Premarket Application for a genetic test for breast cancer (TOP2A FISH pharmDx assay) and granted 510(k) clearance for a cervical disc replacement device (ProDisc-C) and a digital cystoscope (CST-5000 flexible video cystoscope). Medscape Medical News
Category Articles > Business of Medicine
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Date Jan 23, 2008
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