510(k) K983161 ยท ELR Post, Root Canal
KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOC
| Applicant | Sabre-K , Ltd., Cheshire Wa 15 8ah, GB |
| Decision | Substantially Equivalent, Sep 30, 1998 |
| Received | Sep 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983161
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.