510(k) K162556 ยท GEX Powered Laser Surgical Instrument
LIGHTFUSION LED SYSTEM
| Applicant | Vitage Led, Ltd., Basildon, GB |
| Decision | Substantially Equivalent, Mar 24, 2017 |
| Received | Sep 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162556
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.