Medical Device Manufacturer · US , Washington , DC

Deep Breeze , Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Deep Breeze , Ltd. Anesthesiology ✕

3 devices

1-3 of 3

Cleared Mar 04, 2010

VRLXP, MODEL XP

Anesthesiology · 266d

Cleared Oct 15, 2008

Anesthesiology · 300d

Cleared Jul 18, 2007

VR LUNG ELECTROSONOGRAPH

Anesthesiology · 413d