Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K831344Substantially Equivalent

Differentia/diagnostic Occlusa/applianc

Brimms, Inc., Mchenry IL / Traditional, Substantially Equivalent

K831344 is the FDA 510(k) clearance record for DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC, cleared for Brimms, Inc. on . FDA records list 2 510(k) clearances for Brimms, Inc., from to . As of , FDA records show no recalls naming K831344.

Clearance record

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