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Radiation Biodosimetry Medical Countermeasure Devices
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Meeting Notice: May 24, 2016 Circulatory System Devices Panel of the Medical Devices Advisory Committee
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No.FDA-2016-N-0001] Circulatory System Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. ACTION: Notice. This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be…
Class I Medical Device Recall: Focus Diagnostics Recalls Laboratory Examination Kits Due to Inaccurate Test Results
Lot Numbers: 2140887, 2140332, 2127423, 2159531, 2165240, 2173319, 2169601, 2176090, 2181518, 2181519, 2198924, 2163486, 2171337, 2176091, 29230, 29232, 29233, 29453, 29670, 29691, 29671, 29845, 29847, 29848, 29690, 29669, 29692, 29846, 151682, 151685, 151686, 151871, 151918, 151996, 151997, 152055, 152107, 152108, 152359, 151917, 151915, 151995, 151998, 152057, 152056
Class I Medical Device Recall: Vascular Solutions Recalls Guardian II Hemostasis Valve Due to Low Pressure Seal Defect
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Summary Information for: Cheatham Platinum (CP) Stent System (Models 425, 427, 436, 428, and 420/420.1)
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Summary Information for: HeartLight Endoscopic Ablation System
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Summary Information for: Medtronic Micra™ Transcatheter Pacemaker System (Pacemaker Model MC1VR01 and Programmer Application
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Summary Information for: PROPEL® Mini Sinus Implant
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Summary Information for: Cheatham Platinum (CP) Stent System (Models 425, 427, 426, 428, and 420/420.1)
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