510(k) K820215 ยท EJK Liner, Cavity, Calcium Hydroxide
IMPROVED DYCAL
| Applicant | Dentsply Intl., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 23, 1982 |
| Received | Jan 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820215
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.