Amemo, Inc.
Country not established
- Devices
- 1
What Amemo, Inc. makes
Amemo, Inc. manufactures the Fingertip Pulse Oximeter A310, a Class II medical device used for measuring blood oxygen saturation and pulse rate.
The company is based in the US, and its products are listed in the FDA 510(k) registry, which regulates Class II medical devices.
Catalogue
Fingertip Pulse Oximeter A310 Ref K153021
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amemo, Inc. have in the registry?
The registry currently lists 1 device for Amemo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amemo, Inc.'s devices?
Among its 1 most recently registered device, Amemo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Amemo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Amemo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amemo, Inc. in the registry?
The most recently registered devices listed for Amemo, Inc. include Fingertip Pulse Oximeter A310.