510(k) K134022 ยท EJK Liner, Cavity, Calcium Hydroxide
BASE IT
| Applicant | Spident Co., Ltd., Fort Lee NJ, US |
| Decision | Substantially Equivalent, Jun 11, 2014 |
| Received | Dec 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K134022
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.