510(k) K900204 ยท FRN Pump, Infusion
AVI MODEL 840 DUAL CHANNEL INFUSION PUMP
| Applicant | 3M Company, St. Paul MN, US |
| Decision | Substantially Equivalent, Apr 3, 1990 |
| Received | Jan 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900204
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.