Intl. Diagnostic Technology is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Diagnostic Technology - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Intl. Diagnostic Technology has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1976 to 1985. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Intl. Diagnostic Technology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Diagnostic Technology
29 devices
Cleared
Apr 30, 1985
FIAX TOXO-M ANTIBODIES TEST KIT
Microbiology
75d
Cleared
Oct 05, 1984
FIAX HAPTOGLOBIN TEST KIT
Immunology
24d
Cleared
Sep 28, 1984
FIAX 420 DILUTOR
Chemistry
14d
Cleared
Sep 17, 1984
FIAX 100 FLUOROMETER
Immunology
21d
Cleared
Aug 28, 1984
FIAX TOTAL IGE TEST KIT
Immunology
46d
Cleared
Jul 11, 1984
FIAX TRANSFERRIN TEST KIT
Immunology
49d
Cleared
Jun 07, 1984
RUBELLA ANTIBODY FLUOROIMMUNOASSAY
Microbiology
80d
Cleared
May 11, 1984
ALPHA-1-ANTITRYPSIN, FITC, ANTIGEN
Immunology
74d
Cleared
Jan 20, 1984
ANTINUCLEAR ANTIBODY IMMUNOLOGICAL SYS
Immunology
51d
Cleared
Jan 04, 1984
ANTINUCLEAR ANTIBODY IMMUNOLOGICAL
Immunology
48d
Cleared
Oct 14, 1983
FIAX IGG TEST
Immunology
56d
Cleared
Aug 31, 1983
IDT ANA STIQ ASSAY
Immunology
43d