510(k) K994180 ยท LBH Varnish, Cavity
PULPDENT CAVITY PREPARATION III
| Applicant | Pulpdent Corp., Watertown MA, US |
| Decision | Substantially Equivalent, Mar 2, 2000 |
| Received | Dec 10, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994180
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.