510(k) K143316 ยท DQX Wire, Guide, Catheter
Attain Hybrid Guide Wire
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Mar 11, 2015 |
| Received | Nov 19, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143316
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.