Cavitat Medical Technologies, Inc.
Country not established
- Devices
- 1
What Cavitat Medical Technologies, Inc. makes
Cavitat Medical Technologies, Inc. manufactures the CAVITAT ULTRASOUND BONE DENSITOMETER, a Class II medical device used for measuring bone density via ultrasound.
The CAVITAT device is listed in the FDA 510(k) regulatory registry, and the company is based in the United States.
Catalogue
Cavitat Ultrasound Bone Densitometer (Cavitat) Ref K011147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cavitat Medical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Cavitat Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cavitat Medical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Cavitat Medical Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cavitat Medical Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cavitat Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cavitat Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Cavitat Medical Technologies, Inc. include CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT).