Apprise, Inc.
Country not established
- Devices
- 1
What Apprise, Inc. makes
Apprise, Inc. manufactures the INTEGRA(TM) BLOOD GLUCOSE MONITORING SYSTEM, a medical device used for monitoring blood glucose levels.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Integra(Tm) Blood Glucose Monitoring System Ref K893404
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apprise, Inc. have in the registry?
The registry currently lists 1 device for Apprise, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apprise, Inc.'s devices?
Among its 1 most recently registered device, Apprise, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Apprise, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Apprise, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apprise, Inc. in the registry?
The most recently registered devices listed for Apprise, Inc. include INTEGRA(TM) BLOOD GLUCOSE MONITORING SYSTEM.