Devices and Diagnostics Consulting Group
Country not established
- Devices
- 1
What Devices and Diagnostics Consulting Group makes
The company produces the CROSSLAPS ELISA, an enzyme-linked immunosorbent assay (ELISA) test designed for detecting and quantifying specific antibodies or antigens in biological samples.
The CROSSLAPS ELISA is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.
Catalogue
Crosslaps Elisa Ref K972788
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Devices and Diagnostics Consulting Group have in the registry?
The registry currently lists 1 device for Devices and Diagnostics Consulting Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Devices and Diagnostics Consulting Group's devices?
Among its 1 most recently registered device, Devices and Diagnostics Consulting Group has devices listed in FDA 510(k) (1 device).
What risk classes do Devices and Diagnostics Consulting Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Devices and Diagnostics Consulting Group's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Devices and Diagnostics Consulting Group in the registry?
The most recently registered devices listed for Devices and Diagnostics Consulting Group include CROSSLAPS ELISA.