510(k) K082180 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440
| Applicant | Angelus Industria DE Productos Odontologicos, San Diego CA, US |
| Decision | Substantially Equivalent, Dec 17, 2008 |
| Received | Aug 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082180
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.