510(k) K022641 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
TOKUYAMA REBASE II
| Applicant | Tokuyama America, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 2, 2002 |
| Received | Aug 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022641
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.