Houwers Enterprises, Ltd.
Country not established
- Devices
- 1
What Houwers Enterprises, Ltd. makes
Houwers Enterprises, Ltd. manufactures the Multiplex I, a device designed to deliver interferential current therapy for medical applications.
The Multiplex I is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Multiplex I, Interferential Current Ref K841579
510(k) 510(k)
Frequently asked questions
How many devices does Houwers Enterprises, Ltd. have in the registry?
The registry currently lists 1 device for Houwers Enterprises, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Houwers Enterprises, Ltd.'s devices?
Among its 1 most recently registered device, Houwers Enterprises, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Houwers Enterprises, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Houwers Enterprises, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Houwers Enterprises, Ltd. in the registry?
The most recently registered devices listed for Houwers Enterprises, Ltd. include MULTIPLEX I, INTERFERENTIAL CURRENT.