Medical Device Manufacturer · US , New York , NY

Fenem, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

Recent clearances: MODIFIED CLAIMS FOR FEF(TM) END-TIDAL CO2 DETECTOR, 2ND MODIFICATION OF FEF(TM) END-TIDAL CO2 DETECTOR

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Fenem, Inc. Anesthesiology ✕

5 devices

1-5 of 5

Cleared Sep 18, 1989

MODIFIED CLAIMS FOR FEF(TM) END-TIDAL CO2 DETECTOR

Anesthesiology · 63d

Cleared Jul 20, 1989

2ND MODIFICATION OF FEF(TM) END-TIDAL CO2 DETECTOR

Anesthesiology · 43d

Cleared Oct 21, 1988

MODIFIED FEF(TM) END-TIDAL CO2 DETECTOR

Anesthesiology · 24d

Cleared Sep 29, 1988

MODIFIED TOOB-CHEQ CARBON DIOXIDE GAS ANALYZER

Anesthesiology · 21d

Cleared Sep 26, 1988

FEF(TM) END-TIDAL CO2 DETECTOR

Anesthesiology · 18d