510(k) K964194 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CHASE CURVED LEFT HEART VENT CATHETER
| Applicant | Chase Medical, Inc., Richardson TX, US |
| Decision | Substantially Equivalent, Apr 16, 1997 |
| Received | Oct 21, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964194
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.