Wilfred Kromker GmbH
Country not established
- Devices
- 1
What Wilfred Kromker GmbH makes
Wilfred Kromker GmbH manufactures the Ultrasonic Nebuliser Model 2010, a device designed for aerosolising liquid medications into fine mist for inhalation therapy.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US regulatory system.
Catalogue
Ultrasonic Nebuliser Model 2010 Ref K072136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wilfred Kromker GmbH have in the registry?
The registry currently lists 1 device for Wilfred Kromker GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wilfred Kromker GmbH's devices?
Among its 1 most recently registered device, Wilfred Kromker GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Wilfred Kromker GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wilfred Kromker GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wilfred Kromker GmbH in the registry?
The most recently registered devices listed for Wilfred Kromker GmbH include ULTRASONIC NEBULISER MODEL 2010.