510(k) K802684 ยท EAY Light, Fiber Optic, Dental
HELIOMAT
| 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 K802684
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.