510(k) K801031 ยท DXF Catheter, Septostomy
BLADE SEPTOSTOMY CATHETER
| Applicant | Cook, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 28, 1980 |
| Received | May 1, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801031
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.