Catheter Precision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Catheter Precision, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ledgewood, US.
Historical record: 2 cleared submissions from 2019 to 2020. 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.
2 devices