510(k) K965181 ยท KRA Catheter, Continuous Flush
CES INFUSION CATHETER
| Applicant | Cordis Neurovascular, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Mar 21, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965181
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.