510(k) K970114 ยท EJK Liner, Cavity, Calcium Hydroxide
ULTRACAL XS
| Applicant | Ultradent Products, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Mar 14, 1997 |
| Received | Jan 13, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970114
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.