FDA's clearance of medical devices through the 510(k) process.
- Physical Description: 1 online resource (27 pages) : illustrations
- Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2013.
|General Note:|| Title from title screen (viewed Aug. 8, 2016).
|Bibliography, etc. Note:|| Includes bibliographical references.
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|Subject:||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.