510(k) K170738 ยท GEX Powered Laser Surgical Instrument
InMode Diolaze XL
| Applicant | Inmode MD , Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Aug 7, 2017 |
| Received | Mar 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170738
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.