510(k) K170179 ยท GEX Powered Laser Surgical Instrument
LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity
| Applicant | Lumenis, Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Sep 18, 2017 |
| Received | Jan 19, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170179
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.