510(k) K070279 ยท KRA Catheter, Continuous Flush
MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Mar 14, 2007 |
| Received | Jan 29, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070279
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.