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FDA 510(k) Applications Submitted by JIM QUINN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963190
08/15/1996
QA-40M DEFIBRILLATOR TESTER
METRON U.S., INC.
K963198
08/15/1996
PS-41 6M PATIENT SIMULATOR
METRON U.S., INC.
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