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Public Health Effectiveness of the FDA 510(k) Clearance Process: Balancing Patient Safety and Innovation: Workshop Report

Public Health Effectiveness of the FDA 510(k) Clearance Process: Balancing Patient Safety and Innovation: Workshop Report

Paperback

Medical Reference

ISBN10: 0309158494
ISBN13: 9780309158497
Publisher: Natl Academy Pr
Published: Nov 4 2010
Pages: 140
Weight: 0.55
Height: 0.30 Width: 6.00 Depth: 8.90
Language: English

The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.

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Medical Reference