510(k) K012849 ยท ELR Post, Root Canal
GLASS POST
| Applicant | J. Morita USA, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 27, 2002 |
| Received | Aug 3, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012849
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.