510(k) K013963 ยท DQY Catheter, Percutaneous
MODEL 9210 DELIVERY CATHETER, MODEL 9210
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 28, 2002 |
| Received | Dec 3, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013963
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.