510(k) K023818 ยท KIF Resin, Root Canal Filling
FIBERFILL AGP
| Applicant | Pentron Clinical Technologies, Wallingford CT, US |
| Decision | Substantially Equivalent, Apr 3, 2003 |
| Received | Nov 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023818
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.