Enzo Biochem, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enzo Biochem, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Enzo Biochem, Inc. has 5 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Enzo Biochem, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enzo Biochem, Inc.
5 devices
Cleared
Aug 03, 1988
COLORGENE HSV DNA HYBRIDIZATION TEST
Microbiology
173d
Cleared
Jul 08, 1988
HEMAGEL(TM) TEST FOR FECAL OCCULT BLOOD
Hematology
63d
Cleared
Mar 28, 1988
COLORGENE FLUORESCENT DNA HYBRIDIZATION TEST / CMV
Microbiology
88d
Cleared
Dec 04, 1987
COLORGENE DNA HYBRIDIZATION TEST CMV CONFIRMATION
Microbiology
157d
Cleared
May 26, 1987
COLORGENE DNA HYBRIDIZATION TEST FOR HSV CONFIRMA.
Microbiology
90d