Catheter Precision, Inc. is one of 25942 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Catheter Precision, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIVO (9002), VIVO, VIVO
3
Total
3
Cleared
0
Denied
Catheter Precision, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ledgewood, US.
Latest FDA clearance: Oct 2026. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Catheter Precision, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Catheter Precision, Inc.
3 devices