510(k) K982537 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
TOKUYAMA SOFRELINER
| Applicant | Tokuyama America, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Aug 24, 1998 |
| Received | Jul 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982537
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.