510(k) K111483 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
JOULE CLEARSENSE LASER SYSTEM
| Applicant | Sciton, Inc, Palo Alto CA, US |
| Decision | Substantially Equivalent, Dec 7, 2011 |
| Received | May 31, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111483
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.