Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K780568Substantially Equivalent

Duran Flexible Ring

Hancock Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

K780568 is the FDA 510(k) clearance record for DURAN FLEXIBLE RING, cleared for Hancock Laboratories, Inc. on . FDA records list 5 510(k) clearances for Hancock Laboratories, Inc., from to . As of , FDA records show no recalls naming K780568.

Clearance record

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