510(k) K891237 ยท FRN Pump, Infusion
MODEL 600 SYRINGE PUMP
| Applicant | 3M Company, St. Paul MN, US |
| Decision | Substantially Equivalent, Dec 6, 1989 |
| Received | Mar 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891237
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.