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Panel recommends blood test to detect colon cancer for FDA approval
UPI· 9 hours agoA panel of U.S. Food and Drug Administration advisers on Thursday recommended approval for a new...
FDA panel recommends approval of a blood test for colon cancer
NBC NEWS· 12 hours agoAdvisers to the U.S. Food and Drug Administration on Thursday recommended for the approval of...
FDA classifies Hologic’s recall of BioZorb Marker as Class I
Medical Device Network via Yahoo Finance· 21 hours agoThe US Food and Drug Administration (FDA) has classified the recent Hologic BioZorb Marker recall as...
Guardant Health's blood test to detect deadly colon cancer is under review by the FDA
Quartz· 19 hours agoA U.S. Food and Drug Administration (FDA) advisory committee is meeting today to review a new blood...
FDA approves belimumab autoinjector for pediatric systemic lupus erythematosus
Medical Xpress· 20 hours agoThe U.S. Food and Drug Administration has approved GlaxoSmithKline's 200-mg subcutaneous route of...
Scott Klug on Food and Drug Administration (FDA) | JD Supra
JD Supra· 2 days agoJD Supra is a legal publishing service that connects experts and their content with broader audiences of professionals, journalists and associations. This Privacy Policy describes how JD Supra ...
Blood test to detect colon cancer could move a step closer to FDA approval in the US
WTAE Pittsburgh· 15 hours agoPalo Alto, California-based biotechnology company Guardant Health has applied for U.S. Food and Drug...
Indica Labs’ HALO AP Dx platform receives FDA 510(k) clearance
Medical Device Network via Yahoo Finance· 21 hours agoIndica Labs has received 510(k) clearance from the US Food and Drug Administration (FDA) for its...
Hologic recalls more than 53,000 radiographic markers linked to 71 injuries
MedTech Dive via Yahoo Finance· 24 hours agoDive Brief: Hologic has recalled more than 53,000 radiographic markers linked to 71 reported...
Guardant colon cancer test struggles to detect non-cancerous tumors, FDA says
MedTech Dive via Yahoo Finance· 2 days agoA Food and Drug Administration advisory panel will evaluate whether a blood test from Guardant...