510(k) K864300 ยท DYN Mouthpiece, Saliva Ejector
SILIVA EJECTOR/ORAL CAVITY EVACUATOR
| Applicant | Ardent Intl., Inc., Newtown Square PA, US |
| Decision | Substantially Equivalent, Nov 24, 1986 |
| Received | Oct 31, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864300
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.