510(k) K030922 ยท LBH Varnish, Cavity
VIVASENS
| Applicant | Ivoclar Vivadent, Inc., Amherst NY, US |
| Decision | Substantially Equivalent, Oct 17, 2003 |
| Received | Mar 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030922
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.