510(k) K060418 ยท DQY Catheter, Percutaneous
8F SHERPA NX GUIDE CATHETER
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Mar 15, 2006 |
| Received | Feb 17, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060418
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.