Dextron, Inc.
Country not established
- Devices
- 1
What Dextron, Inc. makes
Dextron, Inc. manufactures the DIATRON blood glucose meter, a device used for measuring glucose levels in blood samples to assist in diabetes management.
The DIATRON blood glucose meter is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Diatron Blood Glucose Meter Ref K855178
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dextron, Inc. have in the registry?
The registry currently lists 1 device for Dextron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dextron, Inc.'s devices?
Among its 1 most recently registered device, Dextron, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dextron, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dextron, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dextron, Inc. in the registry?
The most recently registered devices listed for Dextron, Inc. include DIATRON BLOOD GLUCOSE METER.