# Cardiac Resucitator Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 17 (1981–1988): 17 510(k) clearances
- Product codes: DRO (13), MKJ (1), DSI (1), LDO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K882513: Modified Heart*Aid 97 Auto. External Defibrillator (Jul 12, 1988)
- K871538: Stat-Pad (TM) (Jun 24, 1987)
- K871971: Modified Pace*Aid Model 53 (Jun 24, 1987)
- K871569: Modified Heart*Aid 97 Auto. External Defibrillator (Jun 8, 1987)
- K870622: Heart*Aid 1000 (Apr 10, 1987)
- K850596: Pace*Aid 10 a -Pad 10A- Pacemaker Output Display & (Mar 6, 1985)
- K850170: Heart Aid Model 97 (Feb 14, 1985)
- K844811: Pace Aid Model 53 (Jan 24, 1985)

Source page: https://510kreport.com/company/cardiac-resucitator