Midwest Development
Country not established
- Devices
- 1
What Midwest Development makes
Midwest Development manufactures the FT2000 Sequencer, a device designed to control and coordinate electrical stimulation sequences for muscle stimulators. This product is intended for therapeutic applications requiring precise timing and modulation of stimulation pulses.
The FT2000 Sequencer is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
FT2000 Sequencer For Muscle Stimulator Ref K050595
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midwest Development have in the registry?
The registry currently lists 1 device for Midwest Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midwest Development's devices?
Among its 1 most recently registered device, Midwest Development has devices listed in FDA 510(k) (1 device).
What risk classes do Midwest Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Midwest Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midwest Development in the registry?
The most recently registered devices listed for Midwest Development include FT2000 SEQUENCER FOR MUSCLE STIMULATOR.