FDA's clearance of medical devices through the 510(k) process.

Bibliographic Details
Corporate Author: United States. Department of Health and Human Services. Office of Inspector General (Author)
Language:English
Published: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2013.
Subjects:
Medical instruments and apparatus > Government policy > United States.
Medical instruments and apparatus > United States > Classification.
Medical instruments and apparatus > Technological innovations > Government policy > United States.
Genre:
Classification.
Online Access:
Connect to online resource - All users (Federal Depository Library Program Persistant URL)
Physical Description:1 online resource (27 pages) : illustrations
Variant Title:
Food and Drug Administration's clearance of medical devices through the 510(k) process
FDA's clearance of medical devices through the 510(k) process
Format: Government Document Electronic eBook
Description
Note:Title from title screen (viewed Aug. 8, 2016).
"September 2013."
"OEI-04-10-00480."
Call Number:HE 1.75:OEI-04-10-00480 Online
Bibliography Note:Includes bibliographical references.