Medical Device Manufacturer · US , Los Angeles , CA

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

2 submissions · 2 cleared · Since 1997

Recent clearances: SEEMOR 5.0 IMAGE DISPLAY PROGRAM, SEEMOR - DISPLAY & PROCESSING PROGRAM EXECUTING ON PERSONAL COMPUTER SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Aug 16, 2004

SEEMOR 5.0 IMAGE DISPLAY PROGRAM

Radiology · 46d

Cleared Dec 12, 1997

SEEMOR - DISPLAY & PROCESSING PROGRAM EXECUTING ON PERSONAL COMPUTER SYSTEM

Radiology · 78d