Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K801129Substantially Equivalent

Quicktan Booth

Quicktan Mfg., Mchenry IL / Traditional, Substantially Equivalent

K801129 is the FDA 510(k) clearance record for QUICKTAN BOOTH, cleared for Quicktan Mfg. on . FDA records list one 510(k) clearance for Quicktan Mfg. As of , FDA records show no recalls naming K801129.

Clearance record

Decision date
Received
(49 days to decision)
Review panel
Unknown
Applicant
Quicktan Mfg. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No