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International Medical Device Regulatory Monitor
> 510(k) Flow Chart Explains U.S. FDA Review Process
International Medical Device Regulatory Monitor
February 2012
| Vol.
20 No.
2
510(k) Flow Chart Explains U.S. FDA Review Process
Concerns about the future of the U.S. Food and Drug Administration’s (FDA) 510(k) process appear to have been put to rest with the recent issuance of a draft guidance on evaluating substantial equivalence in 510(k)s.
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