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MDUFA Moves to House Floor, Decision Summaries for Some 510(k)s Likely
Fri, 05/11/2012 - 2:30pm
U.S. Food & Drug Administration
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Minutes from Stakeholder Meeting on MDUFA III Reauthorization, February 28, 2012
Guidance for Industry and Food and Drug Administration Staff- FDA and Industry Actions on Premarket Notification (510(k)) Submissions: Effect on FDA Review Clock and Goals
Guidance for Industry and Food and Drug Administration Staff- User Fees and Refunds for Premarket Notification Submissions (510(k)s)
View the discussion thread.
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