Microtech Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Microtech Medical, Inc. makes
Microtech Medical, Inc. makes blood glucose monitoring systems, including the GoChek Blood Glucose Monitoring System and the GoChek Connect Blood Glucose Monitoring System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Informer Plus Ref K943481
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microtech Medical, Inc. have in the registry?
The registry currently lists 2 devices for Microtech Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microtech Medical, Inc.'s devices?
Among its 2 most recently registered devices, Microtech Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Microtech Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Microtech Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microtech Medical, Inc. in the registry?
The most recently registered devices listed for Microtech Medical, Inc. include INFORMER PLUS and GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System.