510(k) K860775 ยท DTP Defoamer, Cardiopulmonary Bypass
MEDIASTINAL AUTOTRANSFUSION SYSTEM
| Applicant | Cardio Metrics, Inc., Houston TX, US |
| Decision | Substantially Equivalent, May 28, 1986 |
| Received | Mar 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860775
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.