Medtronic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae, Retrograde Coronary Sinus Perfusion Cannulae, Clearview Intracoronary Shunts
209
Total
208
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic, Inc. General Hospital ✕
1 devices