510(k) K884845 ยท DZE Implant, Endosseous, Root-Form
STERI-OSS
| Applicant | Denar Corp., Anaheim CA, US |
| Decision | Substantially Equivalent, Feb 10, 1989 |
| Received | Nov 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884845
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.