510(k) K811113 ยท DZA Drill, Dental, Intraoral
RIESS-LUHR
| Applicant | Allomedic, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 16, 1981 |
| Received | Apr 23, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811113
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.