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- 2012405517 alternative "FDA 510(k) clearance process".
- 2012405517 contributor B12575778.
- 2012405517 contributor B12575779.
- 2012405517 date "2010".
- 2012405517 description "Includes bibliographical references.".
- 2012405517 extent "xii, 128 pages :".
- 2012405517 identifier "0309158494 (pbk.)".
- 2012405517 identifier "9780309158497 (pbk.)".
- 2012405517 issued "2010".
- 2012405517 language "eng".
- 2012405517 spatial "United States".
- 2012405517 subject "2011 C-414".
- 2012405517 subject "610 22".
- 2012405517 subject "Device Approval legislation & jurisprudence United States Congresses.".
- 2012405517 subject "Device Approval standards United States Congresses.".
- 2012405517 subject "Equipment Safety standards United States Congresses.".
- 2012405517 subject "Public health Equipment and supplies Standards United States Congresses.".
- 2012405517 subject "Public health United States Congresses.".
- 2012405517 subject "RA399.A3 P818 2010".
- 2012405517 subject "United States. Food and Drug Administration.".
- 2012405517 subject "WB 26".
- 2012405517 title "FDA 510(k) clearance process".
- 2012405517 title "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.".
- 2012405517 type "text".