Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K791050Substantially Equivalent

Centria T3 Uptake Test Set

Ventrex Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

K791050 is the FDA 510(k) clearance record for CENTRIA T3 UPTAKE TEST SET, cleared for Ventrex Laboratories, Inc. on . FDA records list 82 510(k) clearances for Ventrex Laboratories, Inc., from to . As of , FDA records show no recalls naming K791050.

Clearance record

Decision date
Received
(9 days to decision)
Review panel
Unknown
Applicant
Ventrex Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No