Immunomatrix
Country not established
- Devices
- 1
What Immunomatrix makes
Immunomatrix produces the Immunomatrix Theophylline Assay System, a diagnostic device designed for measuring theophylline levels in blood or serum to monitor therapeutic drug concentrations in patients.
The company’s portfolio is regulated under FDA Class II devices and is listed in the 510(k) clearance registry. Immunomatrix operates from the United States.
Catalogue
Immunomatrix Theophyline Assay System Ref K911060
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Immunomatrix have in the registry?
The registry currently lists 1 device for Immunomatrix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Immunomatrix's devices?
Among its 1 most recently registered device, Immunomatrix has devices listed in FDA 510(k) (1 device).
What risk classes do Immunomatrix's devices fall under?
Among its 1 most recently registered device, the classes recorded for Immunomatrix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Immunomatrix in the registry?
The most recently registered devices listed for Immunomatrix include IMMUNOMATRIX THEOPHYLINE ASSAY SYSTEM.