Invivo Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Invivo Corp. has 4 FDA 510(k) cleared medical devices. Based in Pewaukee, US.
Historical record: 4 cleared submissions from 2005 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Invivo Corp. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Dec 15, 2009
MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214
Cardiovascular
267d
Cleared
Nov 03, 2005
MODEL BBD BREAST IMMOBILIZATION AND BIOPSY DEVICE
Radiology
36d
Cleared
Oct 12, 2005
NEUROVASCULAR ARRAY COIL, MODEL NVA-127-16-A
Radiology
30d
Cleared
Jun 28, 2005
CAC-127-8 CARDOAC ARRAY COIL
Radiology
21d