510(k) K172407 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
Duracetal
| Applicant | The Myerson Company Limited, Laventille, TT |
| Decision | Substantially Equivalent, Nov 2, 2017 |
| Received | Aug 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172407
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.