510(k) K962835 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
HEARTPORT ENDOVENOUS DRAINAGE CANNULA
| Applicant | Heartport, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 10, 1997 |
| Received | Jul 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962835
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.