National Diagnostic Products
AustraliaFDA applicant, unverified
- Devices
- 1
What National Diagnostic Products makes
National Diagnostic Products manufactures the BETACHEK GLUCOSE TEST, a device designed for measuring blood glucose levels, typically used for diabetes management.
The BETACHEK GLUCOSE TEST is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Betachek Glucose Test Ref K062187
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does National Diagnostic Products have in the registry?
The registry currently lists 1 device for National Diagnostic Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list National Diagnostic Products's devices?
Among its 1 most recently registered device, National Diagnostic Products has devices listed in FDA 510(k) (1 device).
What risk classes do National Diagnostic Products's devices fall under?
Among its 1 most recently registered device, the classes recorded for National Diagnostic Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from National Diagnostic Products in the registry?
The most recently registered devices listed for National Diagnostic Products include BETACHEK GLUCOSE TEST.