510(k) K894681 ยท DXE Catheter, Embolectomy
REVISED LABELING FOR ARTERIAL EMBOLECTOMY CATHETER
| Applicant | Shiley, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 12, 1989 |
| Received | Jul 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894681
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.