510(k) K964230 ยท FMF Syringe, Piston
CORELIFE
| Applicant | Core Healthcare , Ltd., Battle Creek MI, US |
| Decision | Substantially Equivalent, Jul 24, 1997 |
| Received | Oct 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964230
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.