510(k) K012307 ยท EBF Material, Tooth Shade, Resin
LUXACORE/LUXACORE DUAL
| Applicant | Dmg USA, Inc., Ayer MA, US |
| Decision | Substantially Equivalent, Aug 23, 2001 |
| Received | Jul 23, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K012307
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.