510(k) K103391 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
IVOBASE HYBRID, IVOBASE HIGH IMPACT
| Applicant | Ivoclar Vivadent, Inc., Amherst NY, US |
| Decision | Substantially Equivalent, Feb 17, 2011 |
| Received | Nov 19, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103391
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.