510(k) K093547 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
PINPOINTE FOOTLASER
| Applicant | Pinpointe USA, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Oct 15, 2010 |
| Received | Nov 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093547
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.