Enzyme Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enzyme Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Enzyme Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Nashua, US.
Historical record: 5 cleared submissions from 1989 to 1992. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Enzyme Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enzyme Technology, Inc.
5 devices
Cleared
Jan 30, 1992
CALCIUM (ARSENAZO III) REAGENT, UNIVERSAL
Chemistry
267d
Cleared
Dec 18, 1991
URIC ACID (URICASE) REAGENT, UNIVERSAL
Chemistry
224d
Cleared
Mar 11, 1991
GLUCOSE (HK) REAGENT, UNIVERSAL
Chemistry
111d
Cleared
Dec 11, 1990
TRIGLYCERIDE (GPO) REAGENT, UNIVERSAL
Chemistry
21d
Cleared
Dec 12, 1989
CHOLESTEROL, UNIVERSAL ET
Chemistry
54d