510(k) K101771 ยท EBP Reliner, Denture, Over The Counter
RELINE-IT MODEL RELINE-IT
| Applicant | Majestic Drug Co., Inc., Orange CT, US |
| Decision | Substantially Equivalent, Sep 20, 2010 |
| Received | Jun 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101771
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.