510(k) K942562 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
PROSTHOFLEX
| Applicant | Knopf Assoc, Inc., Livingston NJ, US |
| Decision | Substantially Equivalent, Dec 20, 1994 |
| Received | May 31, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942562
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.