Associates IN Biofeedback
Country not established
- Devices
- 1
What Associates IN Biofeedback makes
Associates IN Biofeedback manufactures electronic perineometers, devices used to measure and monitor pelvic floor muscle function, particularly for clinical assessment and rehabilitation purposes.
The company’s products are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States.
Catalogue
Electronic Perineometer Ref K800303
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Associates IN Biofeedback have in the registry?
The registry currently lists 1 device for Associates IN Biofeedback. Devices recorded under merged duplicate company entries are counted once.
Which registries list Associates IN Biofeedback's devices?
Among its 1 most recently registered device, Associates IN Biofeedback has devices listed in FDA 510(k) (1 device).
What risk classes do Associates IN Biofeedback's devices fall under?
Among its 1 most recently registered device, the classes recorded for Associates IN Biofeedback's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Associates IN Biofeedback in the registry?
The most recently registered devices listed for Associates IN Biofeedback include ELECTRONIC PERINEOMETER.