# CathRx, Ltd.

- Location (FDA's records): Rydalmere, AU
- FDA decisions: 2 (2022–2026): 2 510(k) clearances
- Product codes: DRF (2)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Biosense Webster, Inc.: 1 (https://510kreport.com/company/biosense-webster)

## Recent decisions
- K262068: Khelix Magnetic Sensor Electrophysiology Catheter (SS1-*-*-MAG) (Oct 9, 2026)
- K211327: Khelix Steerable Electrophysiology Catheters, Khelix Loop Fixed Electrophysiology Catheters, Khelix Fixed Loop Steerable Electrophysiology Catheters, Khelix Variable Loop Steerable Electrophysiology Catheters (Feb 10, 2022)

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