510(k) K062420 ยท DQY Catheter, Percutaneous
5F SHERPA ACTIVE NX GUIDE CATHETER
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Sep 8, 2006 |
| Received | Aug 18, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062420
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.