510(k) K802301 ยท FRN Pump, Infusion
CORDIS DOW INFUSION PUMP
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 23, 1980 |
| Received | Sep 22, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802301
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.