Seradyn is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seradyn - FDA 510(k) Cleared Devices
Recent clearances: QMS / MULTIGENT VALPROIC ACID REAGENT, PART #396075, QMS DIGOXIN REAGENT SYSTEM ON THE ABBOTT AEROSET SYSTEM
2
Total
2
Cleared
0
Denied
Seradyn has 2 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Seradyn Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seradyn
2 devices