510(k) K183174 ยท DRA Catheter, Steerable
FlexCath Advance Steerable Sheath and Dilator
| Applicant | Medtronic Cryocath, LP, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 26, 2018 |
| Received | Nov 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183174
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.