Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report

The Resource Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report

Label

Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report

Title remainder

balancing patient safety and innovation : workshop report

Statement of responsibility

Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies

Title variation

FDA 510(k) clearance process

Language

eng

Summary

"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."--Resource home page

Cataloging source

N$T

Dewey number

610

Illustrations

illustrations

Index

no index present

Language note

English

LC call number

RA399.A3

LC item number

P83 2010eb

Literary form

non fiction

Nature of contents

dictionaries
bibliography

NLM call number

WB 26

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Context

Work of