510(k) K143292 ยท EJK Liner, Cavity, Calcium Hydroxide
TheraCal DC
| Applicant | Bisco, Inc., Schaumburg IL, US |
| Decision | Substantially Equivalent, Aug 4, 2015 |
| Received | Nov 17, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143292
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.