Medtronic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LINQ II Insertable Cardiac Monitor (ICM) (LNQ22), Affera Integrated Mapping System, VitalFlow Set with Balance™ Biosurface
213
Total
212
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic, Inc. Ear, Nose, Throat ✕
2 devices