510(k) K884865 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
PERMASEAL AND DENTURE SEAL
| Applicant | American Mfg., Inc., Silver Spring MD, US |
| Decision | Substantially Equivalent, Jan 30, 1989 |
| Received | Nov 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884865
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.