Niveus Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Niveus Medical, Inc. makes
Niveus Medical, Inc. manufactures muscle stimulation systems, including the Muscle Stimulation System 110, designed for therapeutic electrical stimulation of skeletal muscles.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Muscle Stimulation System Ref K123642
Regimes: 510(k) Registry: 510(k)Muscle Stimulation System 110 Ref K150742
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Niveus Medical, Inc. have in the registry?
The registry currently lists 2 devices for Niveus Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Niveus Medical, Inc.'s devices?
Among its 2 most recently registered devices, Niveus Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Niveus Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Niveus Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Niveus Medical, Inc. in the registry?
The most recently registered devices listed for Niveus Medical, Inc. include MUSCLE STIMULATION SYSTEM and Muscle Stimulation System 110.