Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K827380Substantially Equivalent

Scanner Type 1846

Bruel & Kjaer Instruments, Inc., Marlborough MA / Traditional, Substantially Equivalent

K827380 is the FDA 510(k) clearance record for SCANNER TYPE 1846, cleared for Bruel & Kjaer Instruments, Inc. on . FDA records list 4 510(k) clearances for Bruel & Kjaer Instruments, Inc., from to . As of , FDA records show no recalls naming K827380.

Clearance record

Decision date
Received
(80 days to decision)
Review panel
Unknown
Applicant
Bruel & Kjaer Instruments, Inc. 185 Forest St., Marlborough MA
Third party review
No