Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K822849Substantially Equivalent

Raaf Dual Lumen Catheter

Quinton, Inc., Walker MI / Traditional, Substantially Equivalent

K822849 is the FDA 510(k) clearance record for RAAF DUAL LUMEN CATHETER, cleared for Quinton, Inc. on . FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show no recalls naming K822849.

Clearance record

Decision date
Received
(67 days to decision)
Review panel
Unknown
Applicant
Quinton, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No