Medical Device Manufacturer · SE , Bjarred

Seebreath AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Seebreath AB Anesthesiology ✕

1 devices

1-1 of 1

Cleared Jul 13, 2012

CAPNODURA COMBI & CAPNODURA PEDI CO2 DETECTOR

Anesthesiology · 288d