510(k) K890024 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
SARNS VENT CATHETER
| Applicant | 3M Company, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Mar 2, 1989 |
| Received | Jan 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890024
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.