510(k) K964430 ยท LFC Device, Caries Detection
PULPDENT SNOOP
| Applicant | Pulpdent Corp., Watertown MA, US |
| Decision | Substantially Equivalent, Jan 17, 1997 |
| Received | Nov 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964430
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.