Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K850246Substantially Equivalent

Master Kit a

Pro-Lab, Inc., Birmingham AL / Traditional, Substantially Equivalent

K850246 is the FDA 510(k) clearance record for MASTER KIT A, cleared for Pro-Lab, Inc. on . FDA records list 27 510(k) clearances for Pro-Lab, Inc., from to . As of , FDA records show no recalls naming K850246.

Clearance record

Decision date
Received
(77 days to decision)
Review panel
Unknown
Applicant
Pro-Lab, Inc. Post Office Box 11276, Birmingham AL
Third party review
No