510(k) K132144 ยท DZE Implant, Endosseous, Root-Form
KERATOR
| Applicant | LK Consulting Group USA, Inc., Fullerton CA, US |
| Decision | Substantially Equivalent, Mar 21, 2014 |
| Received | Jul 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132144
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.