Extension, Inc.
Country not established
- Devices
- 1
What Extension, Inc. makes
Extension, Inc. manufactures clinical alert notification systems designed to provide real-time alerts for patient monitoring in healthcare settings. These devices are intended to integrate with electronic health record systems to notify staff of critical patient status changes, such as vital sign abnormalities or procedural alerts.
The company’s clinical alert notification systems are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. The devices are listed in the FDA’s 510(k) database. Extension, Inc. is based in the United States.
Catalogue
Clinical Alert Notification Ref K130339
510(k) 510(k)
Frequently asked questions
How many devices does Extension, Inc. have in the registry?
The registry currently lists 1 device for Extension, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Extension, Inc.'s devices?
Among its 1 most recently registered device, Extension, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Extension, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Extension, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Extension, Inc. in the registry?
The most recently registered devices listed for Extension, Inc. include CLINICAL ALERT NOTIFICATION.