Cme Telemetrix, Inc.
Country not established
- Devices
- 1
What Cme Telemetrix, Inc. makes
Cme Telemetrix, Inc. manufactures wireless electroencephalography (EEG) recording systems, including the Model W32, designed for continuous or ambulatory monitoring of brain electrical activity.
The company’s wireless EEG systems are classified as Class II devices under FDA regulations and are authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, adhering to U.S. medical device compliance requirements.
Catalogue
Wireless Eeg Recording System Model W32 Ref K963195
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cme Telemetrix, Inc. have in the registry?
The registry currently lists 1 device for Cme Telemetrix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cme Telemetrix, Inc.'s devices?
Among its 1 most recently registered device, Cme Telemetrix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cme Telemetrix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cme Telemetrix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cme Telemetrix, Inc. in the registry?
The most recently registered devices listed for Cme Telemetrix, Inc. include WIRELESS EEG RECORDING SYSTEM MODEL W32.