Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K827371Substantially Equivalent

Cilco Ascan

Cilco, Inc., Huntington WV / Traditional, Substantially Equivalent

K827371 is the FDA 510(k) clearance record for CILCO ASCAN, cleared for Cilco, Inc. on . FDA records list 5 510(k) clearances for Cilco, Inc., from to . As of , FDA records show no recalls naming K827371.

Clearance record

Decision date
Received
(102 days to decision)
Review panel
Unknown
Applicant
Cilco, Inc. 2205 Fifth St. Rd., Huntington WV
Third party review
No