C.F. Electronics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
C.F. Electronics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Commack, US.
Historical record: 5 cleared submissions from 1992 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by C.F. Electronics, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
May 14, 1996
DRUGBOX
General Hospital
154d
Cleared
Aug 26, 1993
RES Q AIR SYSTEM MODEL HT-1000
Anesthesiology
261d
Cleared
Aug 25, 1993
MARK I HUMIDIFIER
Anesthesiology
90d
Cleared
Jan 27, 1993
THERM O DRUG MODEL HT-747
General Hospital
232d
Cleared
Sep 02, 1992
HOT SACK
General Hospital
162d