510(k) K050038 ยท DQY Catheter, Percutaneous
RELIANT STENT GRAFT BALLOON CATHETER
| Applicant | Medtronic Endovascular Innovations, Santa Rosa CA, US |
| Decision | Substantially Equivalent, Apr 13, 2005 |
| Received | Jan 7, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050038
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.