Winprobe Corporation
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
UltraVision 2 Diagnostic Ultrasound System Ref K173265
Regimes: 510(k) Registry: 510(k)UltraVision 2 Diagnostic Ultrasound System Ref K150580
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Winprobe Corporation have in the registry?
The registry currently lists 2 devices for Winprobe Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Winprobe Corporation's devices?
Among its 2 most recently registered devices, Winprobe Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Winprobe Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Winprobe Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Winprobe Corporation in the registry?
The most recently registered devices listed for Winprobe Corporation include UltraVision 2 Diagnostic Ultrasound System.