Invivo Corporation - FDA 510(k) Cleared Devices
Recent clearances: dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for 1.5T and 3.0T, ds Small Extremity 16Ch Coils for 1.5T and 3.0T, Philips MR Patient Care Portal, DynaCAD
29
Total
29
Cleared
0
Denied
FDA 510(k) Regulatory Record - Invivo Corporation Anesthesiology ✕
1 devices