Campden Medical, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Campden Medical, Ltd. makes
Campden Medical, Ltd. manufactures the Mehesz Stimulating System, a device designed for neuromuscular electrical stimulation to support muscle activation and rehabilitation.
The company’s portfolio is regulated under FDA Class II devices, with the Mehesz Stimulating System listed via a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
The Mehesz Stimulating System Ref K844994
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Campden Medical, Ltd. have in the registry?
The registry currently lists 1 device for Campden Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Campden Medical, Ltd.'s devices?
Among its 1 most recently registered device, Campden Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Campden Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Campden Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Campden Medical, Ltd. in the registry?
The most recently registered devices listed for Campden Medical, Ltd. include THE MEHESZ STIMULATING SYSTEM.