Clinical Information Systems, Inc.
Country not established
- Devices
- 1
What Clinical Information Systems, Inc. makes
Clinical Information Systems, Inc. manufactures the IDS640 Patient Data Display & Storage Monitor, a device designed for capturing, displaying, and storing patient monitoring data in clinical settings.
The IDS640 is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Information Systems, Inc. have in the registry?
The registry currently lists 1 device for Clinical Information Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Information Systems, Inc.'s devices?
Among its 1 most recently registered device, Clinical Information Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Clinical Information Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Clinical Information Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Information Systems, Inc. in the registry?
The most recently registered devices listed for Clinical Information Systems, Inc. include MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT..