Areeda Assoc., Ltd.
Country not established
- Devices
- 2
What Areeda Assoc., Ltd. makes
Areeda Assoc., Ltd. develops medical imaging software, including the SEEMOR 5.0 Image Display Program and SEEMOR processing software designed for execution on personal computer systems. These tools are intended for use in medical environments to display and analyze radiographic images, such as those from computed tomography (CT) or other imaging modalities.
The company’s software portfolio is classified under FDA’s Class II regulatory category and is subject to 510(k) clearance requirements. The devices are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States.
Catalogue
Seemor 5.0 Image Display Program Ref K041782
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Areeda Assoc., Ltd. have in the registry?
The registry currently lists 2 devices for Areeda Assoc., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Areeda Assoc., Ltd.'s devices?
Among its 2 most recently registered devices, Areeda Assoc., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Areeda Assoc., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Areeda Assoc., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Areeda Assoc., Ltd. in the registry?
The most recently registered devices listed for Areeda Assoc., Ltd. include SEEMOR 5.0 IMAGE DISPLAY PROGRAM and SEEMOR - DISPLAY & PROCESSING PROGRAM EXECUTING ON PERSONAL COMPUTER SYSTEM.