510(k) K904979 ยท FRN Pump, Infusion
AVI MODEL 600 SYRINGE PUMP, MODIFICATION
| Applicant | 3M Avi, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jan 15, 1991 |
| Received | Oct 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904979
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.