ECU Libraries Catalog

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

Other author/creatorWizemann, Theresa M.
Other author/creatorInstitute of Medicine (U.S.). Board on Population Health and Public Health Practice.
Other author/creatorInstitute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process.
Format Electronic and Book
Publication InfoWashington, D.C. : National Academies Press, [2010]
Descriptionxii, 128 pages : illustrations (some color) ; 23 cm
Supplemental Content Full text available from Ebook Central - Academic Complete
Portion of title FDA 510(k) clearance process
Abstract "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."-- Source other than Library of Congress.
Bibliography noteIncludes bibliographical references.
Access restrictionAvailable only to authorized users.
Technical detailsMode of access: World Wide Web
Genre/formElectronic books.
LCCN 2012405517
ISBN9780309158497 (pbk.)
ISBN0309158494 (pbk.)

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