Invivo Corporation - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
FDA 510(k) cleared devices by Invivo Corporation Radiology ✕
19 devices
Cleared
Dec 23, 2021
dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for...
Radiology
22d
Cleared
Aug 02, 2021
DynaCAD
Radiology
21d
Cleared
Dec 27, 2019
UroNav System
Radiology
21d
Cleared
Oct 09, 2019
DynaCAD
Radiology
57d
Cleared
Oct 19, 2018
UroNav (Version 3.0)
Radiology
31d
Cleared
Sep 14, 2016
dS FootAnkle I6CH 1.5T Coil
Radiology
41d
Cleared
Aug 31, 2016
1.5T and 3.0T 16 CH GE Shoulder Coils
Radiology
42d
Cleared
Nov 16, 2015
UroNav (Version 2.0)
Radiology
25d
Cleared
Jan 22, 2014
DYNACAD/PROSTATE INTERVENTIONAL (DYNALOC/PROSTATE)
Radiology
118d
Cleared
Dec 21, 2012
SENSE HEAD 16 MODEL 800647, SENSE SPINE 16 MODEL 800646
Radiology
91d
Cleared
Nov 02, 2012
DS BREAST 16CH I/T 1.5T DS BREAST 16CH I/T 3.0T
Radiology
64d
Cleared
Feb 10, 2012
SENSE MSK S 8CH 1.5T
Radiology
24d