Compleware Corp.
Country not established
- Devices
- 1
What Compleware Corp. makes
Compleware Corp. manufactures Clindatalink Version 1.0, a software-based system designed for spirometry data collection, analysis, and reporting. This device integrates with spirometers to capture lung function test results, store patient data, and generate clinical reports for diagnostic evaluation.
The company’s spirometry software is classified as Class II under FDA regulations and is authorised via 510(k) clearance. The product is listed in the FDA’s regulatory database, and the manufacturer operates from the United States.
Catalogue
Clindatalink Version 1.0 For Spirometry Ref K020004
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Compleware Corp. have in the registry?
The registry currently lists 1 device for Compleware Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Compleware Corp.'s devices?
Among its 1 most recently registered device, Compleware Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Compleware Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Compleware Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Compleware Corp. in the registry?
The most recently registered devices listed for Compleware Corp. include CLINDATALINK VERSION 1.0 FOR SPIROMETRY.