510(k) K915268 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CATHETER TWO STAGE VENOUS RETURN
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Jul 27, 1992 |
| Received | Nov 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915268
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.