510(k) K896907 ยท LDR Controller, Infusion, Intravascular, Electronic
3M IV FLOW REGULATOR
| Applicant | 3M Company, St. Paul MN, US |
| Decision | Substantially Equivalent, Feb 26, 1990 |
| Received | Dec 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896907
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.