Home » Controversial 510(k) Proposals Deferred to IOM for Review
Controversial 510(k) Proposals Deferred to IOM for Review
February 9, 2011
Devicemakers may have to wait several months longer to learn whether, or how, the U.S. Food and Drug Administration (FDA) will implement a number of controversial suggestions for revamping its 510(k) clearance process.
To View This Article:
Subscribe To International Medical Device Regulatory Monitor