510(k) K103626 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
CUTERA GENESISPLUS LASER SYSTEM
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Apr 5, 2011 |
| Received | Dec 10, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103626
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.