Medical Device Manufacturer · US , Ledgewood , NJ

Catheter Precision, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2019

Recent clearances: VIVO (9002), VIVO, VIVO

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Catheter Precision, Inc. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Oct 30, 2026

Cardiovascular · 147d

Cleared Sep 14, 2020

Cardiovascular · 221d

Cleared CT Jun 14, 2019

Cardiovascular · 207d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Nov 06, 2026