Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K761102Substantially Equivalent

Ney-Lite

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

K761102 is the FDA 510(k) clearance record for NEY-LITE, 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 K761102.

Clearance record

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