510(k) K123014 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
LITECURE THERAPY SYSTEM MODEL LTS-1500
| Applicant | Litecure, LLC, Newark DE, US |
| Decision | Substantially Equivalent, Mar 29, 2013 |
| Received | Sep 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123014
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.