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FDA 510(k) Applications Submitted by MICHAEL M. KNOTT, M.D.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971354
04/11/1997
KNOTT NG TUBE
MICHAEL M. KNOTT, M.D.
K981966
06/04/1998
NOSEBLEED NOSECLIP
MICHAEL M. KNOTT, M.D.
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