International Enzymes, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
International Enzymes, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
International Enzymes, Inc. has 7 FDA 510(k) cleared medical devices. Based in Fallbrook, US.
Historical record: 7 cleared submissions from 1994 to 2001. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by International Enzymes, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - International Enzymes, Inc.
7 devices
Cleared
May 18, 2001
HSCRP CONTROL LEVEL 1, HSCRP CONTROL LEVEL 2, AND HSCRP CONTROL LEVEL 3
Chemistry
31d
Cleared
Aug 20, 1996
LIQUID IMMUNOLOGY CONTROL LEVEL I, II, III
Chemistry
12d
Cleared
Sep 15, 1995
LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY...
Immunology
31d
Cleared
Sep 15, 1995
LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN...
Immunology
31d
Cleared
Jun 01, 1995
LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - FOR BECKMAN ARRAY 360 SYSTEM
Immunology
100d
Cleared
Dec 02, 1994
LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - E
Immunology
80d
Cleared
Dec 02, 1994
LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E
Immunology
78d