510(k) K170073 ยท GEX Powered Laser Surgical Instrument
LightMed Dental Laser System
| Applicant | Lightmed Dentaltechnology Corp., Kaohsiung, TW |
| Decision | Substantially Equivalent, Jul 25, 2017 |
| Received | Jan 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170073
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.