Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report /
"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 balanc...
| Corporate Authors: | , |
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| Other Authors: | |
| Format: | Book |
| Language: | English |
| Published: |
Washington, D.C. :
National Academies Press,
[2010], ©2010
Washington, D.C. : [2010] |
| Series: | Online access: NCBI NCBI Bookshelf
Online access: National Academy of Sciences National Academies Press |
| Subjects: |