Teltec Electronic Equipment AB
Country not established
- Devices
- 1
What Teltec Electronic Equipment AB makes
Teltec Electronic Equipment AB manufactures the Glottal Frequency Analyser, a device designed for assessing vocal fold function by analyzing fundamental frequency and related parameters in speech or voice signals.
The Glottal Frequency Analyser is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Glottal Frequency Analyser Ref K841832
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teltec Electronic Equipment AB have in the registry?
The registry currently lists 1 device for Teltec Electronic Equipment AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teltec Electronic Equipment AB's devices?
Among its 1 most recently registered device, Teltec Electronic Equipment AB has devices listed in FDA 510(k) (1 device).
What risk classes do Teltec Electronic Equipment AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Teltec Electronic Equipment AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teltec Electronic Equipment AB in the registry?
The most recently registered devices listed for Teltec Electronic Equipment AB include GLOTTAL FREQUENCY ANALYSER.