Janssen Biochimica
Country not established
- Devices
- 1
What Janssen Biochimica makes
Janssen Biochimica manufactures the HUMAN IGG SUBCLASS RID KIT, a diagnostic test used to identify immunoglobulin G (IgG) subclasses in human serum or plasma. This kit aids in the assessment of immune function and potential deficiencies by detecting IgG subclasses 1 through 4.
The HUMAN IGG SUBCLASS RID KIT is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Human Igg Subclass Rid Kit Ref K915650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Janssen Biochimica have in the registry?
The registry currently lists 1 device for Janssen Biochimica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Janssen Biochimica's devices?
Among its 1 most recently registered device, Janssen Biochimica has devices listed in FDA 510(k) (1 device).
What risk classes do Janssen Biochimica's devices fall under?
Among its 1 most recently registered device, the classes recorded for Janssen Biochimica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Janssen Biochimica in the registry?
The most recently registered devices listed for Janssen Biochimica include HUMAN IGG SUBCLASS RID KIT.