510(k) K905312 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS
| Applicant | Baxter Bentley Laboratories, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 15, 1991 |
| Received | Nov 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905312
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.