Synapse Electroceutical Limited
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
What Synapse Electroceutical Limited makes
Synapse Electroceutical Limited manufactures the Synapse Transcutaneous Electrical Stimulation Device, which is a Class II medical device used for transcutaneous electrical stimulation.
The company is based in the US and its device is listed in the FDA 510(k) registry, indicating it is a Class II device cleared for market distribution.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Synapse Electroceutical Limited have in the registry?
The registry currently lists 1 device for Synapse Electroceutical Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synapse Electroceutical Limited's devices?
Among its 1 most recently registered device, Synapse Electroceutical Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Synapse Electroceutical Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Synapse Electroceutical Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Synapse Electroceutical Limited in the registry?
The most recently registered devices listed for Synapse Electroceutical Limited include Synapse Transcutaneous Electrical Stimulation Device.