Medical Device Manufacturer · US , Pewaukee , WI

Invivo Corporation - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 2005

Total

Cleared

Denied

Invivo Corporation has 29 FDA 510(k) cleared medical devices. Based in Pewaukee, US.

Last cleared in 2021. Active since 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Invivo Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Invivo Corporation

29 devices

1-12 of 29

Cleared Dec 23, 2021

dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for...

K213766 · MOS

Radiology · 22d

Cleared Sep 30, 2021

Philips MR Patient Care Portal

dS FootAnkle I6CH 1.5T Coil

K162177 · MOS

Radiology · 41d

Cleared Aug 31, 2016

1.5T and 3.0T 16 CH GE Shoulder Coils

K162001 · MOS

Radiology · 42d

Cleared Dec 23, 2015

Expression MR400 MRI Patient Monitoring System

K152330 · MWI

Cardiovascular · 127d

DYNACAD/PROSTATE INTERVENTIONAL (DYNALOC/PROSTATE)

K133030 · LLZ

Radiology · 118d

Cleared Aug 30, 2013

MRI PATIENT MONITORING SYSTEM

K132359 · MWI

Cardiovascular · 31d

Invivo Corporation - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Invivo Corporation

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