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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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