Disa Electronics
Country not established
- Devices
- 2
What Disa Electronics makes
Disa Electronics manufactures the Neuromatic 2000, a device used for neuromuscular electrical stimulation, and the Disa Water Cystometer, a tool for assessing bladder function through controlled fluid infusion.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Neuromatic 2000 Ref K821237
Regimes: 510(k) Registry: 510(k)Disa Water Cystometer Ref K820144
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Disa Electronics have in the registry?
The registry currently lists 2 devices for Disa Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Disa Electronics's devices?
Among its 2 most recently registered devices, Disa Electronics has devices listed in FDA 510(k) (2 devices).
What risk classes do Disa Electronics's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Disa Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Disa Electronics in the registry?
The most recently registered devices listed for Disa Electronics include NEUROMATIC 2000 and DISA WATER CYSTOMETER.