510(k) K971019 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CHASE VESSEL CANNULA
| Applicant | Chase Medical, Inc., Richardson TX, US |
| Decision | Substantially Equivalent, Jul 21, 1997 |
| Received | Mar 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971019
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.