Kegelmaster 2000, Ltd.
Country not established
- Devices
- 1
What Kegelmaster 2000, Ltd. makes
Kegelmaster 2000, Ltd. manufactures the Kegelmaster 2000, a device designed for pelvic floor muscle training.
The Kegelmaster 2000 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Kegelmaster 2000 Ref K023305
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kegelmaster 2000, Ltd. have in the registry?
The registry currently lists 1 device for Kegelmaster 2000, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kegelmaster 2000, Ltd.'s devices?
Among its 1 most recently registered device, Kegelmaster 2000, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Kegelmaster 2000, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kegelmaster 2000, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kegelmaster 2000, Ltd. in the registry?
The most recently registered devices listed for Kegelmaster 2000, Ltd. include KEGELMASTER 2000.