Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K820208Substantially Equivalent

Zyme a

Dms Laboratories, Mchenry IL / Traditional, Substantially Equivalent

K820208 is the FDA 510(k) clearance record for ZYME A, cleared for Dms Laboratories on . FDA records list 23 510(k) clearances for Dms Laboratories, from to . As of , FDA records show no recalls naming K820208.

Clearance record

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