510(k) K930939 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
REBARON LC
| Applicant | GC America, Inc., Alsip IL, US |
| Decision | Substantially Equivalent, Jan 21, 1994 |
| Received | Feb 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930939
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.