510(k) K143758 ยท DZE Implant, Endosseous, Root-Form
PerioType Rapid
| Applicant | Clinical House Europe GmbH, Bassersdorf, CH |
| Decision | Substantially Equivalent, Aug 7, 2015 |
| Received | Dec 31, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143758
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.