510(k) K771692 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
TUBING SETS
| Applicant | Cobe Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1977 |
| Received | Sep 6, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771692
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.