510(k) K001050 ยท EJK Liner, Cavity, Calcium Hydroxide
CALCIJECT
| Applicant | Centrix, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jul 21, 2000 |
| Received | Mar 31, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001050
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.