Medical Device Manufacturer · US , Greenville , SC

Vidistar, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Vidistar, LLC has 2 FDA 510(k) cleared medical devices. Based in Greenville, US.

Historical record: 2 cleared submissions from 2009 to 2015. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Vidistar, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vidistar, LLC

2 devices

1-2 of 2