510(k) K953079 ยท EJK Liner, Cavity, Calcium Hydroxide
LIMELIGHT
| Applicant | Pulpdent Corp., Watertown MA, US |
| Decision | Substantially Equivalent, Aug 7, 1995 |
| Received | Jul 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953079
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.