510(k) K981009 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
HEARTPORT ENDOPULMONARY VENT CATHETER
| Applicant | Heartport, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Sep 4, 1998 |
| Received | Mar 18, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981009
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.