510(k) K113843 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
FREEDOM ND: YAG LASER SYSTEM
| Applicant | Lutronic Corporation, Trevose PA, US |
| Decision | Substantially Equivalent, Sep 27, 2012 |
| Received | Dec 28, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113843
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.