FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX

K Number: K984582 · Decision Mar 16, 1999
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
227
Applicant Total
17
Review Days
83

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Basic Information

Device Name
ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX
K Number
K984582
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Detek, Inc.
Date Received
December 23, 1998
Decision Date
March 16, 1999
Product Code
MKJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MKJ Automated External Defibrillators (Non-Wearable)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MKJ), ordered by most recent decision date.

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Other Clearances by Bio-Detek, Inc.

K Number Device Name
K150198 CPR Dura-Padz Reusable Defibrillation Electrode with Dura-padz Gel
K150055 OneStep Pediatric CPR Multi-Function Electrode
K133441 ONESTEP CPR II MULTI-FUNCTION ELECTRODE
K100565 DURA PADZ (REUSABLE ELECTRODE), DURA PADZ GEL (DISPOSABLE HYDROGEL) MODEL 8900-0300, 8900-0325
K071321 POCKETCPR
K040256 PEDI-PADZ RADIOLUCENT MULTI-FUNCTION PEDIATRIC ELECTRODES, MODEL 8900-1005
K040056 BIO-DETEK ELECTRODE ADAPTER, MODEL R2001-90
K033771 BIO-DETEK MODIFIED ADULT MULTI-FUNCTION ELECTRODE WITH CONNECTOR
K990106 ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES
K981802 ZOLL STAT*PADZ ADULT MULTI-FUNCTION ELECTRODES MODEL NUMBER 8900-4003
Search all 17 clearances from Bio-Detek, Inc. →