Medical Device Manufacturer · US , Commack , NY

C.F. Electronics, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Recent clearances: DRUGBOX, RES Q AIR SYSTEM MODEL HT-1000, MARK I HUMIDIFIER

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - C.F. Electronics, Inc. Anesthesiology ✕

2 devices

1-2 of 2

Cleared Aug 26, 1993

RES Q AIR SYSTEM MODEL HT-1000

Anesthesiology · 261d

Cleared Aug 25, 1993

MARK I HUMIDIFIER

Anesthesiology · 90d