510(k) K760894 ยท DWD Suction Control, Intracardiac, Cardiopulmonary Bypass
VACUUM RELIEF VALVE
| Applicant | Delta Medical Industries, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 9, 1976 |
| Received | Oct 26, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760894
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.