510(k) K102821 ยท LFC Device, Caries Detection
DISCOVRED
| Applicant | Phoenix Dental, Inc., Fenton MI, US |
| Decision | Substantially Equivalent, Mar 11, 2011 |
| Received | Sep 28, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102821
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.