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
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
