Microware, Inc.
Country not established
- Devices
- 1
What Microware, Inc. makes
Microware, Inc. manufactures the MICROWARE 200, a Class II medical device designed for [specific function or application—if not provided, omit or clarify if generic; here, no functional detail is given, so omit].
The MICROWARE 200 is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Microware 200 Ref K050740
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microware, Inc. have in the registry?
The registry currently lists 1 device for Microware, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microware, Inc.'s devices?
Among its 1 most recently registered device, Microware, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Microware, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Microware, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microware, Inc. in the registry?
The most recently registered devices listed for Microware, Inc. include MICROWARE 200.