TY - BOOK AU - Institute of Medicine A2 - Theresa Wizemann TI - Public Health Effectiveness of the FDA 510(k) Clearance Process: Balancing Patient Safety and Innovation: Workshop Report SN - 978-0-309-15849-7 DO - 10.17226/12960 PY - 2010 UR - https://nap.nationalacademies.org/catalog/12960/public-health-effectiveness-of-the-fda-510k-clearance-process-balancing PB - The National Academies Press CY - Washington, DC LA - English KW - Health and Medicine AB - 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. ER -