510(k) K970638 ยท DXC Clamp, Vascular
CTS MIDCAB FIXEDN DIAMETER CORONARY SHUNT
| Applicant | Cardiothoracic Systems, Inc., Cupertino CA, US |
| Decision | Substantially Equivalent, Oct 30, 1997 |
| Received | Feb 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970638
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.