Meditek Technology, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Blood Pressure Monitor, Model M100 Ref K032308
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meditek Technology, Inc. have in the registry?
The registry currently lists 1 device for Meditek Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meditek Technology, Inc.'s devices?
Among its 1 most recently registered device, Meditek Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Meditek Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Meditek Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meditek Technology, Inc. in the registry?
The most recently registered devices listed for Meditek Technology, Inc. include BLOOD PRESSURE MONITOR, MODEL M100.