Eyetect, LLC
Country not established
- Devices
- 1
What Eyetect, LLC makes
Eyetect, LLC manufactures the Eyetect Tremor Monitor Unit (TMU), a device designed for monitoring tremor activity in patients, likely for clinical or diagnostic purposes.
The TMU is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Eyetect Tremor Monitor Unit (Tmu) Ref K003644
510(k) 510(k)
Frequently asked questions
How many devices does Eyetect, LLC have in the registry?
The registry currently lists 1 device for Eyetect, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyetect, LLC's devices?
Among its 1 most recently registered device, Eyetect, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Eyetect, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eyetect, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eyetect, LLC in the registry?
The most recently registered devices listed for Eyetect, LLC include EYETECT TREMOR MONITOR UNIT (TMU).