Medical Device Manufacturer · US , Denton , TX

Mevisys Co., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Mevisys Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Denton, US.

Historical record: 2 cleared submissions from 2002 to 2005. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Mevisys Co., Ltd.

2 devices

1-2 of 2