# Cardiorhythm

- Location (FDA's records): San Jose, CA
- FDA decisions: 2 (1993–1993): 2 510(k) clearances
- Product codes: DRF (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Innovative Health, LLC: 1 (https://510kreport.com/company/innovative-health)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K923915: Torqr Series Diagnostic EP Catheters (1993), cited by 2

## Recent decisions
- K923916: Voyagr Series Diagnostic EP Catheters (Feb 10, 1993)
- K923915: Torqr Series Diagnostic EP Catheters (Feb 10, 1993)

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