510(k) K190753 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
EverCrossTM 0.035 OTW PTA Dilatation Catheter
| Applicant | Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.), Plymouth MN, US |
| Decision | Substantially Equivalent, Apr 23, 2019 |
| Received | Mar 25, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190753
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.