Cardio-Phoenix, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cardio-Phoenix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cardio-TriTest v6.5
2
Total
2
Cleared
0
Denied
Cardio-Phoenix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio-Phoenix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardio-Phoenix, Inc.
2 devices