Atlas FDA

ZAP-GUARD

FDA 510(k) clearance K896985 · decided 1990-07-31

Clearance details

K-number
K896985
Device name
ZAP-GUARD
Applicant
Guardian Angel Products, Inc.
Decision
Substantially Equivalent
Date received
1989-12-13
Decision date
1990-07-31
Days to decision
230 days
Clearance type
Traditional
Product code
DRL
Device class
2
Regulation number
870.5325
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Huntingdon Valley, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Delta 3300 (K190437)Netech Corporation2019-08-28
UniPulse (K182905)Seaward Group2018-12-14
Defibrillator Analyzer Variable Load (K153210)Bc Group International, Inc.2015-12-21
DEFIBRILLATOR ANALYZER - DA-2006P (K110192)Bc Group International, Inc.2011-02-08
IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADS (K083347)Fluke Biomedical2008-12-24
IMPULSE 6000D/7000DP (K072114)Fluke Biomedical2008-01-28
PHASE 3, MODEL DT-1 (K062099)Datrend Systems, Inc.2007-01-25
MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE (K030547)Guardian Angel Products, Inc.2003-07-11
QA-40M DEFIBRILLATOR TESTER (K963190)Metron U.S., Inc.1997-07-01
DEFIBRILLATOR ANALYZER, DELTA 1000 (K961595)Netech Corp.1996-10-29
MODELS QED-6, 6M AND 6H DEFIBRILLATOR ANALYZER WITH OPTIONAL UNIVERSAL PACEMAKER LOAD ADAPTER (K954391)Bio-Tek Instruments, Inc.1995-11-17
IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER (K941404)Hogan & Hartson1994-06-29

Recalls involving this device

No recalls on record reference this clearance.