510(k) K173067 ยท GEX Powered Laser Surgical Instrument
LightForce LTS Model 1000, 1500, 2500, and 4000
| Applicant | Litecure, LLC, Newark DE, US |
| Decision | Substantially Equivalent, Feb 22, 2018 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173067
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.