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

HEART*AID 1000

K Number: K870622 · Decision Apr 10, 1987
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
227
Applicant Total
17
Review Days
57

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Basic Information

Device Name
HEART*AID 1000
K Number
K870622
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cardiac Resucitator Corp.
Date Received
February 12, 1987
Decision Date
April 10, 1987
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 Cardiac Resucitator Corp.

K Number Device Name
K882513 MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
K871971 MODIFIED PACE*AID MODEL 53
K871538 STAT-PAD (TM)
K871569 MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
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. →