Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K827760Substantially Equivalent

Digital Fluorographic X-Ray System

General Electric Co., Schenectady NY / Traditional, Substantially Equivalent

K827760 is the FDA 510(k) clearance record for DIGITAL FLUOROGRAPHIC X-RAY SYSTEM, 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 K827760.

Clearance record

Decision date
Received
(20 days to decision)
Review panel
Unknown
Applicant
General Electric Co. 1 River Rd., Schenectady NY
Third party review
No