510(k) K963503 ยท DXC Clamp, Vascular
CTS MIDCAB CORONARY SHUNT
| Applicant | Cardiothoracic Systems, Inc., Cupertino CA, US |
| Decision | Substantially Equivalent, Apr 3, 1997 |
| Received | Sep 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963503
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.