Dako A/S
Country not established
- Devices
- 2
What Dako A/S makes
Dako A/S manufactures diagnostic products including cystatin C immunoparticles, control sets, and calibrators. The company also produces the Dakocytomation beta-2-microglobulin kit.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dako A/S have in the registry?
The registry currently lists 2 devices for Dako A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dako A/S's devices?
Among its 2 most recently registered devices, Dako A/S has devices listed in FDA 510(k) (2 devices).
What risk classes do Dako A/S's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dako A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dako A/S in the registry?
The most recently registered devices listed for Dako A/S include CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR and DAKOCYTOMATION BETA-2-MICROGLOBULIN KIT, CODE NO. OA 368.