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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