Kronus is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kronus - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Kronus has 4 FDA 510(k) cleared medical devices. Based in Dana Point, US.
Historical record: 4 cleared submissions from 1989 to 1992. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kronus Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kronus
4 devices
Cleared
Mar 30, 1992
KRONUS KALIBRE THYROGLOBULIN ANTIBODY EIA KIT
Immunology
119d
Cleared
Mar 30, 1992
KRONUS KALIBRE THYROID PEROXIDASE ANTIBODY EIA KIT
Immunology
119d
Cleared
Jul 25, 1989
ANTI-THYROGLOBULIN TEST KIT
Immunology
36d
Cleared
Jul 25, 1989
MODIFIED KRONUS TEST KIT FOR ANTIBODIES TO (TPO)
Immunology
11d