510(k) K970113 ยท EJK Liner, Cavity, Calcium Hydroxide
ULTRA-BLEND PLUS
| Applicant | Ultradent Products, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Jan 13, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970113
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.