510(k) K170060 ยท GEX Powered Laser Surgical Instrument
M22 and ResurFx Systems
| Applicant | Lumenis, Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Aug 9, 2017 |
| Received | Jan 6, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170060
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.