510(k) K961594 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
BETTER-VENTER
| Applicant | Circulatory Technology, Inc., Oyster Bay NY, US |
| Decision | Substantially Equivalent, Sep 5, 1996 |
| Received | Apr 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961594
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.