510(k) K173827 ยท GEX Powered Laser Surgical Instrument
LightScalpel
| Applicant | Lightscalpel, LLC, Bothell WA, US |
| Decision | Substantially Equivalent, Sep 14, 2018 |
| Received | Dec 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173827
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.