510(k) K103810 ยท DZE Implant, Endosseous, Root-Form
KJ SUBMERGED SYSTEM
| Applicant | Kj Meditech Co., Ltd., Fullerton CA, US |
| Decision | Substantially Equivalent, Sep 14, 2011 |
| Received | Dec 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103810
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.