510(k) K801401 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CARDIOPULMONARY BYPASS TUBING
| Applicant | Texas Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 30, 1980 |
| Received | Jun 13, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801401
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.