FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR

K Number: K882513 · Decision Jul 12, 1988
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
17
Review Days
40

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Basic Information

Device Name
MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
K Number
K882513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cardiac Resucitator Corp.
Date Received
June 2, 1988
Decision Date
July 12, 1988
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

Similar 510(k) Clearances

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

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Other Clearances by Cardiac Resucitator Corp.

K Number Device Name
K871971 MODIFIED PACE*AID MODEL 53
K871538 STAT-PAD (TM)
K871569 MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
K870622 HEART*AID 1000
K850596 PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &
K850170 HEART AID MODEL 97
K844811 PACE AID MODEL 53
K843547 PACE *AID MODEL 52
K843358 HEART-AID MODEL 80
K841556 HEART - AID ALS, 95
Search all 17 clearances from Cardiac Resucitator Corp. →