510(k) K011762 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
HI-WAVE; POUR-PLUS
| Applicant | Denplus, Inc., Longueuil, Quebec, CA |
| Decision | Substantially Equivalent, Aug 23, 2001 |
| Received | Jun 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011762
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.