510(k) K894684 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT
| Applicant | Pioneering Technologies, Inc., Wheat Ridge CO, US |
| Decision | Substantially Equivalent, Oct 17, 1989 |
| Received | Jul 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894684
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.