510(k) K941532 ยท EJK Liner, Cavity, Calcium Hydroxide
BIOCALEX 6/9
| Applicant | Bio-Probe, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Aug 2, 1994 |
| Received | Mar 30, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941532
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.