510(k) K896980 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
PALFIQUE LIGHT LINER
| Applicant | Tokuyama America, Inc., Washington DC, US |
| Decision | Substantially Equivalent, May 15, 1990 |
| Received | Dec 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896980
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.