Seracare Technology is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seracare Technology - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Seracare Technology has 5 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 5 cleared submissions from 1999 to 1999. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Seracare Technology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seracare Technology
5 devices
Cleared
Dec 09, 1999
QUALITROL IMMUNOASSAY PLUS CONTROL, LEVELS 1,2 AND 3
Immunology
100d
Cleared
Dec 09, 1999
QUALITROL TUMOR MARKER CONTROL, LEVELS 1 AND 2
Immunology
43d
Cleared
Nov 16, 1999
QUALITROL CARDIAC MARKER CONTROL, LEVELS, 1,2 AND 3
Immunology
13d
Cleared
Nov 12, 1999
QUALITROL IMMUNOLOGY CONTROL, LEVEL 1, 2 AND 3
Immunology
87d
Cleared
Aug 26, 1999
URINE DRUG SCREENING CONTROL
Toxicology
38d