Dimension Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dimension Diagnostics - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Dimension Diagnostics has 8 FDA 510(k) cleared medical devices. Based in St. Charles, US.
Historical record: 8 cleared submissions from 1985 to 1987. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Dimension Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dimension Diagnostics
8 devices
Cleared
Mar 10, 1987
DIMENSION-WBG
Chemistry
201d
Cleared
Jun 25, 1986
ALT-30, 60 AND 100
Chemistry
75d
Cleared
Jan 07, 1986
CRITIC - SF, ASSAYED
Chemistry
27d
Cleared
Dec 23, 1985
CRITIC C LEVEL I & II
Immunology
90d
Cleared
Jul 22, 1985
UROL-GUANT
Chemistry
54d
Cleared
Mar 01, 1985
IMA-TROL IMMUNOASSAY CONTROL
Chemistry
78d
Cleared
Jan 08, 1985
CRITIC-ARS
Chemistry
36d
Cleared
Jan 08, 1985
UROL-QUAL
Chemistry
32d