Alcatel-Lucent Canada, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Alcatel-Lucent Canada, Inc. makes
Alcatel-Lucent Canada, Inc. develops telehealth management software designed to support remote patient monitoring and clinical workflow integration, including tools for managing patient data and coordinating care delivery.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Alcatel-Lucent Teleheath Manager Ref K092635
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alcatel-Lucent Canada, Inc. have in the registry?
The registry currently lists 1 device for Alcatel-Lucent Canada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alcatel-Lucent Canada, Inc.'s devices?
Among its 1 most recently registered device, Alcatel-Lucent Canada, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alcatel-Lucent Canada, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alcatel-Lucent Canada, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alcatel-Lucent Canada, Inc. in the registry?
The most recently registered devices listed for Alcatel-Lucent Canada, Inc. include ALCATEL-LUCENT TELEHEATH MANAGER.