510(k) K061735 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
INFIBRA, MODEL 1200
| Applicant | Global Dental Products, Inc., Wantagh NY, US |
| Decision | Substantially Equivalent, Sep 8, 2006 |
| Received | Jun 20, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061735
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.