# CATHRX

FEI: 3014368660
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: CathRx (#10084686)

Address: Unit 8, 2-8 South St, Rydalmere New South Wales, 2116, AU

Mandatory US Agent: Acorn N Oakes LLC

## Products

Total registered: 1
Top product codes: DRF
Regulation §: 870.1220

Proprietary names: Khelix Fixed Electrophysiology Catheter, Khelix Fixed Loop Steerable Electrophysiology Catheters, Khelix Variable Loop Steerable Electrophysiology Catheters, Khelix Loop Electrophysiology Catheter, Khelix Steerable Electrophysiology Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014368660%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014368660