Remote Diagnostic Technologies, Ltd. A Philips Company
United KingdomFDA applicant, unverified
- Devices
- 1
What Remote Diagnostic Technologies, Ltd. A Philips Company makes
Remote Diagnostic Technologies, Ltd. manufactures the Tempus LS, a manual device designed for temperature monitoring and diagnostic purposes.
The Tempus LS is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Tempus LS - Manual Ref K200849
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Remote Diagnostic Technologies, Ltd. A Philips Company have in the registry?
The registry currently lists 1 device for Remote Diagnostic Technologies, Ltd. A Philips Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remote Diagnostic Technologies, Ltd. A Philips Company's devices?
Among its 1 most recently registered device, Remote Diagnostic Technologies, Ltd. A Philips Company has devices listed in FDA 510(k) (1 device).
What risk classes do Remote Diagnostic Technologies, Ltd. A Philips Company's devices fall under?
Among its 1 most recently registered device, the classes recorded for Remote Diagnostic Technologies, Ltd. A Philips Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Remote Diagnostic Technologies, Ltd. A Philips Company in the registry?
The most recently registered devices listed for Remote Diagnostic Technologies, Ltd. A Philips Company include Tempus LS - Manual.