510(k) K896139 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
SR-IVOSEAL
| Applicant | Ivoclar North America, Inc., Amherst NY, US |
| Decision | Substantially Equivalent, Apr 16, 1990 |
| Received | Oct 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896139
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.