# Cardiotronics, Inc.

- Location (FDA's records): West Carlsbad, CA
- FDA decisions: 27 (1988–1995): 27 510(k) clearances
- Product codes: LDD (14), DRO (9), DRX (2), GXD (1), DPS (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- ZOLL Medical Corporation: 1 (https://510kreport.com/company/zoll-medical)

## Its most-cited devices
- K883375: Model #918 Multi-Pads (1988), cited by 1

## Recent decisions
- K932903: Ekg Vest (Feb 24, 1995)
- K922064: Model #510 Stealth-Plate Dispersive Electrode (Dec 1, 1992)
- K923297: Model #340 Stealth-Trode+LS (Sep 18, 1992)
- K922227: Model #225-ST Shock-Trode Adult Defib Pads Sterile (Jun 11, 1992)
- K922173: Model # 830 ST Adult Stimulation Pads (Sterile) (Jun 11, 1992)
- K922172: Model # 230 ST Stealth-Trode Defib Pads (Sterile) (Jun 11, 1992)
- K921606: Model #125 Child Stimulation Pads (May 26, 1992)
- K920086: Shock-Patch Adult Defibrillation Pads (Feb 3, 1992)

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