Promatek
CanadaFDA applicant, unverified
- Devices
- 1
What Promatek makes
Promatek manufactures the ES 180-DCM, a muscle stimulator designed for therapeutic or rehabilitative use, targeting muscle activation and recovery.
The ES 180-DCM is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Es 180-Dcm Muscle Stimulator Ref K860619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promatek have in the registry?
The registry currently lists 1 device for Promatek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promatek's devices?
Among its 1 most recently registered device, Promatek has devices listed in FDA 510(k) (1 device).
What risk classes do Promatek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Promatek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promatek in the registry?
The most recently registered devices listed for Promatek include ES 180-DCM MUSCLE STIMULATOR.