Akos Biomedical, Inc.
Country not established
- Devices
- 1
What Akos Biomedical, Inc. makes
Akos Biomedical, Inc. manufactures endoscopes, which are flexible or rigid tubes equipped with a light and camera to visualize internal body structures for diagnostic and therapeutic procedures.
The company’s endoscopes are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Endoscope Ref K964131
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Akos Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Akos Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Akos Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Akos Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Akos Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Akos Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Akos Biomedical, Inc. in the registry?
The most recently registered devices listed for Akos Biomedical, Inc. include ENDOSCOPE.