FDA 510(k) Applications Submitted by Medtronic, Inc. (formerly d.b.a. ev3 Inc, Covidien llc.)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190753 | 03/25/2019 | EverCrossTM 0.035 OTW PTA Dilatation Catheter | Medtronic, Inc. (formerly d.b.a. ev3 Inc, Covidien llc.) |
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