Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K854339Substantially Equivalent

Cui Chin Sizer

Cox-Uphuff Intl., Santa Barbara CA / Traditional, Substantially Equivalent

K854339 is the FDA 510(k) clearance record for CUI CHIN SIZER, cleared for Cox-Uphuff Intl. on . FDA records list 11 510(k) clearances for Cox-Uphuff Intl., from to . As of , FDA records show no recalls naming K854339.

Clearance record

Decision date
Received
(18 days to decision)
Review panel
Unknown
Applicant
Cox-Uphuff Intl. 725 E. Yanonali St., Santa Barbara CA
Third party review
No