Delta Marketing, Inc.
Country not established
- Devices
- 1
What Delta Marketing, Inc. makes
Delta Marketing, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the DS-200 and DS-400 models, designed for pain management and muscle stimulation.
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
Ds-200 And Ds-400 T.E.N.S. Ref K881832
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Delta Marketing, Inc. have in the registry?
The registry currently lists 1 device for Delta Marketing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Delta Marketing, Inc.'s devices?
Among its 1 most recently registered device, Delta Marketing, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Delta Marketing, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Delta Marketing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Delta Marketing, Inc. in the registry?
The most recently registered devices listed for Delta Marketing, Inc. include DS-200 AND DS-400 T.E.N.S..