Wistron Corporation
TaiwanFDA applicant, unverified
- Devices
- 2
What Wistron Corporation makes
Wistron Corporation manufactures the BESTSHAPE Blood Pressure Monitoring System, a device designed for continuous or intermittent measurement of blood pressure, and the HEALTHTRACKER, a wearable health monitoring device for tracking vital signs and activity metrics.
These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Bestshape Blood Pressure Monitoring System Ref K112647
Regimes: 510(k) Registry: 510(k)Healthtracker Ref K110770
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wistron Corporation have in the registry?
The registry currently lists 2 devices for Wistron Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wistron Corporation's devices?
Among its 2 most recently registered devices, Wistron Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Wistron Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wistron Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wistron Corporation in the registry?
The most recently registered devices listed for Wistron Corporation include BESTSHAPE BLOOD PRESSURE MONITORING SYSTEM and HEALTHTRACKER.