Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K770172Substantially Equivalent

Pellet, Calibration

Deringer-Ney, Inc., Mchenry IL / Traditional, Substantially Equivalent

K770172 is the FDA 510(k) clearance record for PELLET, CALIBRATION, cleared for Deringer-Ney, Inc. on . FDA records list 46 510(k) clearances for Deringer-Ney, Inc., from to . As of , FDA records show no recalls naming K770172.

Clearance record

Decision date
Received
(12 days to decision)
Review panel
Unknown
Applicant
Deringer-Ney, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No