510(k) K910568 ยท DTP Defoamer, Cardiopulmonary Bypass
MODEL 5866-46 SLEEVE KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 9, 1991 |
| Received | Feb 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910568
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.