Ams Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ams Diagnostics - FDA 510(k) Cleared Devices
Recent clearances: LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600
1
Total
1
Cleared
0
Denied
Ams Diagnostics has 1 FDA 510(k) cleared medical devices. Based in Weston, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ams Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ams Diagnostics
1 devices