bio_subbu
Super Moderator
US FDA Issued a guidance document Guidance for Industry and FDA Staff - User Fees and Refunds for Premarket Notification Submissions (510(k)s), issued on August 27, 2009.
This document supersedes “User Fees and Refunds for Premarket Notification Submissions (510(k)s)” dated May 28, 2004.
Regards
S. Subramaniam
This document supersedes “User Fees and Refunds for Premarket Notification Submissions (510(k)s)” dated May 28, 2004.
Regards
S. Subramaniam
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