Medical Device Manufacturer · US , Rockville , MD

Deltex Medical - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1995

Recent clearances: DP240 240 HOUR DOPPLER PROBE, CARDIOQ, MODEL 9051-7005, EDM

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Deltex Medical Cardiovascular ✕

3 devices

1-3 of 3

Cleared Mar 08, 2006

DP240 240 HOUR DOPPLER PROBE

Cardiovascular · 135d

Cleared Aug 06, 2003

CARDIOQ, MODEL 9051-7005

Cardiovascular · 65d

Cleared Nov 07, 1995

Cardiovascular · 225d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 27, 2026