Medical Device Manufacturer · US , Los Angeles , CA

Areeda Assoc., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Areeda Assoc., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 1997 to 2004. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Areeda Assoc., Ltd.

2 devices

1-2 of 2