510(k) K211265 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
TFX-LT2000 Therapy Light
| Applicant | Toefx, Inc., Hamilton, CA |
| Decision | Substantially Equivalent, Nov 17, 2022 |
| Received | Apr 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211265
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.