FDA 510(k) Applications Submitted by PAUL MASON

FDA 510(k) Number Submission Date Device Name Applicant
K120781 03/15/2012 CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH FUJI SYSTEMS CORP.
K954714 10/02/1995 AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION) PACESETTER, INC.


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