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Class I Medical Device Recall: Abbott Vascular Recalls MitraClip Clip Delivery System Due to Issue with Delivery System Deployment Process
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FDA Medical Device 2015 Quality System Data
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Summary Information for: GORE® EXCLUDER® Iliac Branch Endoprosthesis
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Olympus Validates Updated Reprocessing Instructions for Duodenoscope Models TJF-160F and TJF-160VF: FDA Safety Communication
Date Issued: March 15, 2016 Audience: Users of the Olympus TJF-160F and TJF-160VF duodenoscopes and reprocessing facilities including: Gastroenterologists Gastrointestinal surgeons Endoscopy nurses Staff working in endoscopy reprocessing units in health care facilities Infection control practitioners Facility risk managers Medical Specialties: Gastroenterology, Infection Control Device: Olympus duodenoscope models TJF-160F and TJF-160VF Olympus Corporation of the…
Presentations posted for March 15, 2016 Circulatory System Devices Panel of the Medical Devices Advisory Committee Meeting
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Summary Information for: SAPIEN XT Transcatheter Heart Valve and Accessories
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Transcript posted for February 19, 2016 Orthopaedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee
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Letter to Texas Children’s Hospital and Houston Methodist Hospital regarding the Zika Direct Test
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Meeting materials posted for March 15, 2016 Circulatory System Devices Panel of the Medical Devices Advisory Committee Meeting
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