510(k) K873882 ยท EJK Liner, Cavity, Calcium Hydroxide
ALKALINER
| Applicant | Espe GmbH (Us), Lake Worth FL, US |
| Decision | Substantially Equivalent, Feb 26, 1988 |
| Received | Sep 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873882
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.