510(k) K802683 ยท EBF Material, Tooth Shade, Resin
HELIOSIT
| Applicant | Vivadent (Usa), Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 24, 1980 |
| Received | Oct 28, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802683
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.