Ats Co.
Country not established
- Devices
- 1
What Ats Co. makes
Ats Co. manufactures the Digital EMG Monitor Myotron 120, a device used for electromyography (EMG) testing to assess muscle and nerve function by recording electrical activity.
The Myotron 120 is classified as Class II under FDA regulations and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Digital Emg Monitor Myotron 120 Ref K882266
510(k) 510(k)
Frequently asked questions
How many devices does Ats Co. have in the registry?
The registry currently lists 1 device for Ats Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ats Co.'s devices?
Among its 1 most recently registered device, Ats Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Ats Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ats Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ats Co. in the registry?
The most recently registered devices listed for Ats Co. include DIGITAL EMG MONITOR MYOTRON 120.