510(k) K895290 ยท FPA Set, Administration, Intravascular
CHEMO-SPIKE RECONSTITUTION DEVICE
| Applicant | The Medi-Dose Group, Feasterville PA, US |
| Decision | Substantially Equivalent, Dec 27, 1989 |
| Received | Aug 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895290
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.