# Arrhythmia Technologies, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 2 (1992–1992): 2 510(k) clearances
- Product codes: DRF (2)
- 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
- Alliance Medical Corp.: 1 (https://510kreport.com/company/alliance-medical)

## Its most-cited devices
- K915563: Diagnostic EP Catheter (1992), cited by 1

## Recent decisions
- K915563: Diagnostic EP Catheter (Mar 9, 1992)
- K915640: Voyagr Series of Deflectable Diagostic EP Catheter (Mar 9, 1992)

Source page: https://510kreport.com/company/arrhythmia-technologies