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

HEART-AID MODEL 80

K Number: K843358 · Decision Nov 19, 1984
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
83
Applicant Total
17
Review Days
84

Basic Information

Device Name
HEART-AID MODEL 80
K Number
K843358
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5550
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
CARDIAC RESUCITATOR CORP.
Date Received
August 27, 1984
Decision Date
November 19, 1984
Product Code
DRO
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
DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

Similar 510(k) Clearances

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

View all

Other Clearances by CARDIAC RESUCITATOR CORP.

K Number Device Name
K882513 MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
K871538 STAT-PAD (TM)
K871971 MODIFIED PACE*AID MODEL 53
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
K841556 HEART - AID ALS, 95
Search all 17 clearances from CARDIAC RESUCITATOR CORP. →