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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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