Medical Device Manufacturer · US , Indianapolis , IN

Seradyn - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002
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
1-2 of 2
Cleared Apr 28, 2003
QMS / MULTIGENT VALPROIC ACID REAGENT, PART #396075
K030405 · LEG
Toxicology · 81d
Cleared Oct 24, 2002
QMS DIGOXIN REAGENT SYSTEM ON THE ABBOTT AEROSET SYSTEM
K023058 · KXT
Toxicology · 41d
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