510(k) K994368 ยท LFC Device, Caries Detection
AMERICAN DENTAL PRODUCTS CARIES-DETECTOR PLUS
| Applicant | American Dental Products, Inc., Bensenville IL, US |
| Decision | Substantially Equivalent, Mar 14, 2000 |
| Received | Dec 27, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994368
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.