510(k) K801770 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
ARTERIAL BUBBLE TRAP
| Applicant | Delta Medical Industries, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 7, 1980 |
| Received | Jul 28, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801770
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.