510(k) K951813 ยท LFC Device, Caries Detection
CARIES DETECTOR
| Applicant | Kuraray Co., Washington DC, US |
| Decision | Substantially Equivalent, Jul 11, 1995 |
| Received | Apr 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951813
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.