Diasorin/American Standard Companies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diasorin/American Standard Companies - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Diasorin/American Standard Companies has 1 FDA 510(k) cleared medical devices. Based in Columbia, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diasorin/American Standard Companies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diasorin/American Standard Companies
1 devices