510(k) K925062 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
PERMAFLEX PERMANENT SOFT DENTURE RELINER
| Applicant | Protech Professional Products, Inc., Centereach NY, US |
| Decision | Substantially Equivalent, Mar 31, 1993 |
| Received | Oct 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925062
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.