510(k) K912031 ยท FRN Pump, Infusion
AVI MODEL 870 DUAL CHANNEL INFUSION PUMP
| Applicant | 3M Avi, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jun 18, 1991 |
| Received | May 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912031
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.