FDA 510(k) Applications Submitted by MICHAEL R DUPELLE

FDA 510(k) Number Submission Date Device Name Applicant
K990106 01/12/1999 ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES BIO-DETEK, INC.
K981802 05/21/1998 ZOLL STAT*PADZ ADULT MULTI-FUNCTION ELECTRODES MODEL NUMBER 8900-4003 BIO-DETEK, INC.
K964213 10/22/1996 TRACE RITE SOLID GEL ECG ELECTRODES BIO-DETEK, INC.
K984582 12/23/1998 ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX BIO-DETEK, INC.


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