510(k) K863758 ยท EGD Wax, Dental, Intraoral
ORTHO-BITE WAX WAFER
| Applicant | Columbus Dental Mfg. Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Oct 7, 1986 |
| Received | Sep 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863758
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.