510(k) K043538 ยท KRA Catheter, Continuous Flush
HYPERTRANSIT INFUSION CATHETER
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Apr 18, 2005 |
| Received | Dec 22, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043538
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.