Biosonix, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Biosonix, Ltd. makes
Biosonix, Ltd. makes the Flowguard Device.
The Flowguard Device is a Class II medical device listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Flowguard Device Ref K013803
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biosonix, Ltd. have in the registry?
The registry currently lists 1 device for Biosonix, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosonix, Ltd.'s devices?
Among its 1 most recently registered device, Biosonix, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Biosonix, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biosonix, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biosonix, Ltd. in the registry?
The most recently registered devices listed for Biosonix, Ltd. include FLOWGUARD DEVICE.