# Cardiotronics Systems, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 4 (1996–1997): 4 510(k) clearances
- Product codes: MKJ (3), LDD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 4 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Full Power Aed: 1 (https://510kreport.com/company/full-power-aed)

## Its most-cited devices
- K964469: 700-F Series Stimulation Electrodes (1996), cited by 1

## Recent decisions
- K971148: 700-SP Series Disposable Stimulation Electrodes (May 15, 1997)
- K970719: 700-MP Disposable Radiolucent Multi-Pad Electrodes (Apr 16, 1997)
- K964991: 700-FR Series Radiolucent Stimulation Electrodes (Jan 15, 1997)
- K964469: 700-F Series Stimulation Electrodes (Dec 11, 1996)

Source page: https://510kreport.com/company/cardiotronics-systems