Boditestor
Country not established
- Devices
- 1
What Boditestor makes
Boditestor manufactures the FITKIT I Checkup Kit, a Class I diagnostic device designed for at-home health assessments.
The FITKIT I Checkup Kit is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Fitkit I Checkup Kit Ref K830340
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Boditestor have in the registry?
The registry currently lists 1 device for Boditestor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boditestor's devices?
Among its 1 most recently registered device, Boditestor has devices listed in FDA 510(k) (1 device).
What risk classes do Boditestor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Boditestor's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Boditestor in the registry?
The most recently registered devices listed for Boditestor include FITKIT I CHECKUP KIT.