510(k) K070286 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass
BIO-CONSOLE, MODEL 560
| Applicant | Medtronic, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 22, 2007 |
| Received | Jan 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070286
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.