Back IN Action, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Back IN Action, Inc. makes
Back IN Action, Inc. makes electric massagers and low frequency stimulators, including the PM830 electric massager and the SW 803 low frequency stimulator Dana Touch.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
PM830 Electric Massager Ref K891394
Regimes: 510(k) Registry: 510(k)Sw 803 Low Frequency Stimulator Dana Touch Ref K891458
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Back IN Action, Inc. have in the registry?
The registry currently lists 2 devices for Back IN Action, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Back IN Action, Inc.'s devices?
Among its 2 most recently registered devices, Back IN Action, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Back IN Action, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Back IN Action, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Back IN Action, Inc. in the registry?
The most recently registered devices listed for Back IN Action, Inc. include PM830 ELECTRIC MASSAGER and SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH.