510(k) K913019 ยท ELR Post, Root Canal
PDI PARALLEL SIDED POST KIT
| Applicant | Precident Corp., Chatsworth CA, US |
| Decision | Substantially Equivalent, Oct 2, 1991 |
| Received | Jul 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913019
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.