# CARDIONXT

FEI: 3020036682
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: CardioNXT (#10050640)

Address: 12011 N Tejon St Suite 700, Westminster, CO, US



## Products

Total registered: 1
Top product codes: DQK
Regulation §: 870.1425

Proprietary names: iMap 3d Mapping and Navigation System, Axis Patient Patches, MultiLink CS Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223020036682%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3020036682