Medical Device Manufacturer · US , Irvine , CA

Baxter Bentley Laboratories, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1988

Recent clearances: DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD., DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS, MEMBRANE OXYGENATOR

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Baxter Bentley Laboratories, Inc. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Jan 15, 1991

DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.

Cardiovascular · 48d

Cleared Jan 15, 1991

DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS

Cardiovascular · 48d

Cleared Sep 27, 1988

MEMBRANE OXYGENATOR

Cardiovascular · 78d