Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K827543Substantially Equivalent

Maxicamera Model 200A

General Electric Co., Des Plaines IL / Traditional, Substantially Equivalent

K827543 is the FDA 510(k) clearance record for MAXICAMERA MODEL 200A, cleared for General Electric Co. on . FDA records list 256 510(k) clearances for General Electric Co., from to . As of , FDA records show no recalls naming K827543.

Clearance record

Decision date
Received
(45 days to decision)
Review panel
Unknown
Applicant
General Electric Co. 515 E. Touhy Ave., Des Plaines IL
Third party review
No