Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K827126Substantially Equivalent

Technomed Generator, Radiographic, 3 Phase

Tecnomed, Inc., Richmond VA / Traditional, Substantially Equivalent

K827126 is the FDA 510(k) clearance record for TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE, cleared for Tecnomed, Inc. on . FDA records list 18 510(k) clearances for Tecnomed, Inc., from to . As of , FDA records show no recalls naming K827126.

Clearance record

Decision date
Received
(29 days to decision)
Review panel
Unknown
Applicant
Tecnomed, Inc. 2428 Hanover Ave., Richmond VA
Third party review
No