510(k) K940982 ยท KRD Device, Vascular, For Promoting Embolization
ARTERIAL EMBOLIZATION DEVICE (KRD)
| Applicant | Cook, Inc., Bloomington IN, US |
| Decision | Substantially Equivalent, Oct 14, 1994 |
| Received | Mar 1, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940982
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.