510(k) K082594 ยท LBH Varnish, Cavity
REMESENSE
| Applicant | Remedent NV, Claremont NH, US |
| Decision | Substantially Equivalent, Mar 19, 2009 |
| Received | Sep 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082594
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.