California Integrated Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
California Integrated Diagnostics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
California Integrated Diagnostics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Berkeley, US.
Historical record: 4 cleared submissions from 1987 to 1991. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by California Integrated Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - California Integrated Diagnostics, Inc.
4 devices
Cleared
Feb 01, 1991
HERPES SIMPLEX VIRUS TISSUE CULTURE CONF. TYPING
Microbiology
148d
Cleared
Dec 07, 1987
TRICHOMONAS DIRECT ENZYME IMMUNOASSAY
Microbiology
48d
Cleared
Apr 08, 1987
MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT
Microbiology
8d
Cleared
Apr 08, 1987
MODIFIED TRICHOMONAS DIRECT SPECIMEN TEST KIT
Microbiology
8d