510(k) K180719 ยท GEX Powered Laser Surgical Instrument
InMode Diolaze System
| Applicant | Inmode MD , Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Jun 14, 2018 |
| Received | Mar 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180719
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.