510(k) K230341 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
ACRIFIX
| Applicant | Deltamed GmbH, Friedberg, DE |
| Decision | Substantially Equivalent, Apr 6, 2023 |
| Received | Feb 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230341
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.