Murray Electronics
Country not established
- Devices
- 3
What Murray Electronics makes
Murray Electronics manufactures neurostimulation devices, including the BIONICARE Stimulator System (Model BIO-1000) and the BIONICARE Stimulator (Model BIO-1), designed for targeted nerve or muscle stimulation.
These devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Bionicare Stimulator System. Model Bio-1000 Ref K971437
Regimes: 510(k) Registry: 510(k)Bionicare Stimulator Bio-1 Ref K832805
Regimes: 510(k) Registry: 510(k)Bionicare Stimilator System, Model Bio-1000 Ref K983228
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Murray Electronics have in the registry?
The registry currently lists 3 devices for Murray Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Murray Electronics's devices?
Among its 3 most recently registered devices, Murray Electronics has devices listed in FDA 510(k) (3 devices).
What risk classes do Murray Electronics's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Murray Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Murray Electronics in the registry?
The most recently registered devices listed for Murray Electronics include BIONICARE STIMULATOR SYSTEM. MODEL BIO-1000, BIONICARE STIMULATOR BIO-1 and BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000.