510(k) K142952 ยท GEX Powered Laser Surgical Instrument
InMode Diolaze Device
| Applicant | Inmode MD , Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Jan 13, 2015 |
| Received | Oct 10, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142952
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.