Pantheon Research
Country not established
- Devices
- 1
What Pantheon Research makes
Pantheon Research manufactures electrostimulator devices designed for neuromuscular electrical stimulation (NMES) applications, intended to facilitate muscle activation and rehabilitation.
The company’s portfolio is regulated under FDA Class II (U) devices and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pantheon Electrostimulator Ref K133980
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pantheon Research have in the registry?
The registry currently lists 1 device for Pantheon Research. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pantheon Research's devices?
Among its 1 most recently registered device, Pantheon Research has devices listed in FDA 510(k) (1 device).
What are the newest devices from Pantheon Research in the registry?
The most recently registered devices listed for Pantheon Research include PANTHEON ELECTROSTIMULATOR.