Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K840036Substantially Equivalent

Fitex

Britt Corp., Inc., Chanhassen MN / Traditional, Substantially Equivalent

K840036 is the FDA 510(k) clearance record for FITEX, cleared for Britt Corp., Inc. on . FDA records list 2 510(k) clearances for Britt Corp., Inc. As of , FDA records show no recalls naming K840036.

Clearance record

Decision date
Received
(295 days to decision)
Review panel
Unknown
Applicant
Britt Corp., Inc.
Third party review
No