Ria Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ria Diagnostics - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ria Diagnostics has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1978 to 1986. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ria Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ria Diagnostics
7 devices
Cleared
Jan 24, 1986
T-3 UPTAKE/RIASSAY
Chemistry
38d
Cleared
Jan 15, 1986
T-4 RIASSAY
Chemistry
44d
Cleared
Aug 12, 1985
T-3 RIASSAY
Chemistry
59d
Cleared
Feb 19, 1981
DIGOXIN RIA ASSAY
Toxicology
15d
Cleared
Aug 27, 1980
TSH RIASSAY
Chemistry
35d
Cleared
Feb 25, 1980
THEOPHYLLINE RIASSAY
Toxicology
133d
Cleared
Jan 20, 1978
ANTITHROMBIN III RIA
Hematology
17d