510(k) K092583 ยท NBL Light-Induced Fluorescence Caries Detector
SOPROLIFE
| Applicant | Sopro, Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Aug 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092583
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.