FDA Device Establishments · JSON-LD · Markdown

CARDIONXT

FEI 3020036682 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3020036682
Owner / OperatorCardioNXT (#10050640)
Address12011 N Tejon St Suite 700, Westminster, CO, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DQK
Regulation § (21 CFR)870.1425
Proprietary namesiMap 3d Mapping and Navigation System; Axis Patient Patches; MultiLink CS Catheter

External sources

Source: openFDA. Public-domain (CC0).