510(k) K072479 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
FLEXITE SUPREME, FLEXITE PLUS, FLEXITE M.P., NORTHERN AND FLEXITE PRO-GUARD
| Applicant | Rapid Injection Systems Corp., Sound Beach NY, US |
| Decision | Substantially Equivalent, Nov 9, 2007 |
| Received | Sep 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072479
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.