Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K802262Unknown

Composite Restorative

L.D. Caulk Co., Mchenry IL / Traditional, Unknown

K802262 is the FDA 510(k) clearance record for COMPOSITE RESTORATIVE, cleared for L.D. Caulk Co. on . FDA records list 20 510(k) clearances for L.D. Caulk Co., from to . As of , FDA records show no recalls naming K802262.

Clearance record

Decision date
Received
(0 days to decision)
Review panel
Unknown
Applicant
L.D. Caulk Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No