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Guidance for Industry and Food and Drug Administration Staff – Factors to Consider When Making Benefit
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Patient Preference Information – Voluntary Submission, Review in PMA Applications, HDE Applications, and De Novo Requests, and Inclusion in Decision Summaries and Device Labeling
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Amendment of Notice Announcement : September 15, 2016 National Mammography Quality Assurance Advisory Committee Meeting
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2016-N-0001] National Mammography Quality Assurance Advisory Committee; Amendment of Notice AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing an amendment to the notice of meeting of the National Mammography Quality Assurance Advisory Committee. This…
24 Hour Summary posted for August 16, 2016 Microbiology Devices Panel of the Medical Devices Advisory Committee meeting
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Presentations posted for August 16, 2016 Microbiology Devices Panel of the Medical Devices Advisory Committee meeting
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Public Workshop – Adapting Regulatory Oversight of Next Generation Sequencing-Based Tests
The Food and Drug Administration is announcing the following public workshop entitled: “Adapting Regulatory Oversight of Next Generation Sequencing-Based Tests”. The purpose of this workshop is to obtain feedback on two FDA draft guidances, “Use of Standards in FDA Regulatory Oversight of Next Generation Sequencing (NGS)-Based In Vitro Diagnostics (IVDs) Used for Diagnosing Germline Diseases”…
Consumer Information on: Edwards SAPIEN 3 Transcatheter Heart Valve
This is a brief overview of information related to FDA’s approval to market this product. See the links below to the Summary of Safety and Effectiveness Data (SSED) and product labeling for more complete information on this product, its indications for use, and the basis for FDA’s approval. Product Name: Edwards SAPIEN 3 Transcatheter Heart…
Consumer Information on: Edwards SAPIEN XT Transcatheter Heart Valve
This is a brief overview of information related to FDA’s approval to market this product. See the links below to the Summary of Safety and Effectiveness Data (SSED) and product labeling for more complete information on this product, its indications for use, and the basis for FDA’s approval. Product Name: Edwards SAPIEN XT Transcatheter Heart…
Evaluation of Automatic Class III Designation (De Novo) Summaries (DEN150029 added)
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