American Dade is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Dade - FDA 510(k) Cleared Devices
149
Total
149
Cleared
0
Denied
American Dade has 149 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 149 cleared submissions from 1980 to 1987. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by American Dade Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Dade
149 devices
Cleared
Oct 20, 1987
STRATUS(R) HFSH FLUOROMETRIC ENZYME IMMUNOASSAY
Chemistry
77d
Cleared
Sep 29, 1987
STRATUS(R) CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
Chemistry
49d
Cleared
Sep 14, 1987
STRATUS(R) HLH FLUOROMETRIC ENZYME IMMUNOASSAY
Chemistry
41d
Cleared
Sep 02, 1987
PARAMAX URINE/CSF CALIBRATOR
Chemistry
50d
Cleared
Aug 06, 1987
DATA-FI DIMERTEST LATEX ASSAY
Hematology
59d
Cleared
Jul 31, 1987
AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III
Chemistry
53d
Cleared
Jul 21, 1987
STRATUS IGE FLUOROMETRIC ENZYME IMMUNOASSAY
Immunology
61d
Cleared
Jul 09, 1987
DADE MONI-TROL CHEMISTRY CONTROL/CALIBRATOR
Chemistry
48d
Cleared
Jul 07, 1987
PARAMAX CHOLESTEROL REAGENT
Chemistry
40d
Cleared
Jul 06, 1987
DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
Hematology
18d
Cleared
Mar 19, 1987
STRATUS FREE THYROXINE (FT4) FLUOR. ENZYME IMMUNO.
Chemistry
65d
Cleared
Feb 25, 1987
SMI DIGITRON
Chemistry
22d
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