510(k) K883981 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
GUIDING CATHETER (TIP SOFTNESS CHANGE)
| Applicant | Devices For Vascular Intervention, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Nov 3, 1988 |
| Received | Sep 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883981
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.