Medical Device Manufacturer · US , Columbus , OH

Neoprobe Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neoprobe Corp. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Feb 08, 2005

QUANTIX/OR BLOOD FLOW MONITOR

Cardiovascular · 26d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026