Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K837334Substantially Equivalent

X-Ray Beam Filter

Eastman Kodak Company, Rochester NY / Traditional, Substantially Equivalent

K837334 is the FDA 510(k) clearance record for X-RAY BEAM FILTER, cleared for Eastman Kodak Company on . FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show no recalls naming K837334.

Clearance record

Decision date
Received
(23 days to decision)
Review panel
Unknown
Applicant
Eastman Kodak Company 343 State St., Rochester NY
Third party review
No