Medtest Systems, Inc.
Country not established
- Devices
- 1
What Medtest Systems, Inc. makes
Medtest Systems, Inc. manufactures the MEDISENSOR 2001, a Class II medical device designed for diagnostic or monitoring purposes in clinical settings.
The MEDISENSOR 2001 is regulated under the FDA’s 510(k) pathway and is listed in the U.S. Food and Drug Administration’s device registry. The company is based in the United States.
Catalogue
Medisensor 2001 Ref K903564
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtest Systems, Inc. have in the registry?
The registry currently lists 1 device for Medtest Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtest Systems, Inc.'s devices?
Among its 1 most recently registered device, Medtest Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtest Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtest Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtest Systems, Inc. in the registry?
The most recently registered devices listed for Medtest Systems, Inc. include MEDISENSOR 2001.