Virotherm Laboratory
Country not established
- Devices
- 1
What Virotherm Laboratory makes
Virotherm Laboratory manufactures the VIROTHERM Humidifier, a device designed to deliver moisture therapy for respiratory support.
The company’s portfolio is regulated under FDA’s Class I device classification, with the VIROTHERM Humidifier listed via a 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Virotherm Humidifier Ref K915603
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Virotherm Laboratory have in the registry?
The registry currently lists 1 device for Virotherm Laboratory. Devices recorded under merged duplicate company entries are counted once.
Which registries list Virotherm Laboratory's devices?
Among its 1 most recently registered device, Virotherm Laboratory has devices listed in FDA 510(k) (1 device).
What risk classes do Virotherm Laboratory's devices fall under?
Among its 1 most recently registered device, the classes recorded for Virotherm Laboratory's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Virotherm Laboratory in the registry?
The most recently registered devices listed for Virotherm Laboratory include VIROTHERM HUMIDIFIER.