510(k) K900601 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
SARNS DELPHIN BASE ADAPTER WITH MINI-BATTERY
| Applicant | 3M Company, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Mar 28, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900601
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.