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.

Areeda Assoc., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2