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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