510(k) K903781 ยท FRN Pump, Infusion
AVI MODEL 880 DUAL CHANNEL INFUSION PUMP
| Applicant | 3M Avi, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 30, 1990 |
| Received | Aug 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903781
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.