Medi Consultants, Inc.
Country not established
- Devices
- 1
What Medi Consultants, Inc. makes
Medi Consultants, Inc. manufactures the SHE-LI TENS Stimulator Model SL-101 RX, a transcutaneous electrical nerve stimulation (TENS) device designed for pain management.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
She-Li Tens Stimulator Model Sl-101 Rx Ref K961809
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi Consultants, Inc. have in the registry?
The registry currently lists 1 device for Medi Consultants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi Consultants, Inc.'s devices?
Among its 1 most recently registered device, Medi Consultants, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medi Consultants, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medi Consultants, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi Consultants, Inc. in the registry?
The most recently registered devices listed for Medi Consultants, Inc. include SHE-LI TENS STIMULATOR MODEL SL-101 RX.