Promatek Industries, Ltd.
CanadaFDA applicant, unverified
- Devices
- 3
What Promatek Industries, Ltd. makes
Promatek Industries, Ltd. manufactures electrostimulation devices, including the I.F. and MST models for therapeutic applications, as well as the KINESTIM Muscle Stimulator for muscle activation and rehabilitation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Electrostim I.F. Ref K873566
Regimes: 510(k) Registry: 510(k)Electrostim Mst Ref K901417
Regimes: 510(k) Registry: 510(k)Kinestim Muscle Stimulator Ref K871472
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promatek Industries, Ltd. have in the registry?
The registry currently lists 3 devices for Promatek Industries, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promatek Industries, Ltd.'s devices?
Among its 3 most recently registered devices, Promatek Industries, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Promatek Industries, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Promatek Industries, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promatek Industries, Ltd. in the registry?
The most recently registered devices listed for Promatek Industries, Ltd. include ELECTROSTIM I.F., ELECTROSTIM MST and KINESTIM MUSCLE STIMULATOR.