Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K841718Unknown

Frekatheter Venous Catheterisation Sys

Fresenius USA, Inc., Walker MI / Traditional, Unknown

K841718 is the FDA 510(k) clearance record for FREKATHETER VENOUS CATHETERISATION SYS, cleared for Fresenius USA, Inc. on . FDA records list 38 510(k) clearances for Fresenius USA, Inc., from to . As of , FDA records show no recalls naming K841718.

Clearance record

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