Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K842359Substantially Equivalent

Automatic Patient Chair Pm2000 & a

Planmeca U.S.A. Inc, Mchenry IL / Traditional, Substantially Equivalent

K842359 is the FDA 510(k) clearance record for AUTOMATIC PATIENT CHAIR PM2000 & A, cleared for Planmeca USA, Inc. on . FDA records list 13 510(k) clearances for Planmeca USA, Inc., from to . As of , FDA records show no recalls naming K842359.

Clearance record

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