Public Health Effectiveness of the FDA 510 (k) Clearance Process: Balancing Patient Safety and Innovation: Workshop Report - Institute of Medicine - Books - National Academies Press - 9780309158497 - October 4, 2010
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Institute of Medicine
Public Health Effectiveness of the FDA 510 (k) Clearance Process: Balancing Patient Safety and Innovation: Workshop Report

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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.

140 pages, col. Illustrations

Media Books     Paperback Book   (Book with soft cover and glued back)
Released October 4, 2010
ISBN13 9780309158497
Publishers National Academies Press
Pages 140
Dimensions 152 × 229 × 25 mm   ·   301 g
Editor Wizemann, Theresa

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