Ducker CL
Country not established
- Devices
- 1
What Ducker CL makes
Ducker CL manufactures the Series 600 centrifuge, a laboratory device with four distinct variations designed for separating substances via centrifugal force.
The Series 600 centrifuge is classified as a Class I medical device in the US and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Ducker CL have in the registry?
The registry currently lists 1 device for Ducker CL. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ducker CL's devices?
Among its 1 most recently registered device, Ducker CL has devices listed in FDA 510(k) (1 device).
What risk classes do Ducker CL's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ducker CL's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ducker CL in the registry?
The most recently registered devices listed for Ducker CL include SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE.