Clinical Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clinical Diagnostics, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Clinical Diagnostics, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1977 to 1998. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Clinical Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clinical Diagnostics, Inc.
8 devices
Cleared
Jan 02, 1998
GLUCOCHEK POCKETLAB II BLOOD GLUCOSE SYSTEM
Chemistry
241d
Cleared
Feb 22, 1996
GLUCOCHEK POCKETLAB
Chemistry
330d
Cleared
Jan 17, 1995
GLUCOCHEK
Chemistry
368d
Cleared
Jun 02, 1986
GORDON DIAGNOSTIC SYSTEM MODEL I
Neurology
175d
Cleared
Oct 25, 1977
CENTRIFICHEM SYS 400 ANALYZER
Chemistry
28d
Cleared
Jul 11, 1977
CENTRIA SEPARATION COLUMNS TYPE A
Immunology
20d
Cleared
Jun 23, 1977
CENTRIA CORTISOL RIA
Immunology
2d
Cleared
Mar 16, 1977
CENTRIA T4 RIA
Chemistry
86d