510(k) K991774 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
ACRON MC MODIFICATION
| Applicant | GC America, Inc., Alsip IL, US |
| Decision | Substantially Equivalent, Jul 9, 1999 |
| Received | May 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991774
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.