Sonodyne America, Ltd.
Country not established
- Devices
- 1
What Sonodyne America, Ltd. makes
Sonodyne America, Ltd. manufactures the Patient Temperature Monitor, Model 1000, a device designed to measure and display body temperature for clinical use.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Temperature Monitor, Model 1000 Ref K874159
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonodyne America, Ltd. have in the registry?
The registry currently lists 1 device for Sonodyne America, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonodyne America, Ltd.'s devices?
Among its 1 most recently registered device, Sonodyne America, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sonodyne America, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sonodyne America, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonodyne America, Ltd. in the registry?
The most recently registered devices listed for Sonodyne America, Ltd. include PATIENT TEMPERATURE MONITOR, MODEL 1000.