Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K802223Unknown

Quintrex 0515 Programmable Pulse Gen.

Medcor, Inc., Mchenry IL / Traditional, Unknown

K802223 is the FDA 510(k) clearance record for QUINTREX 0515 PROGRAMMABLE PULSE GEN., cleared for Medcor, Inc. on . FDA records list 8 510(k) clearances for Medcor, Inc., from to . As of , FDA records show no recalls naming K802223.

Clearance record

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