Cronus
Country not established
- Devices
- 3
What Cronus makes
Cronus manufactures in vitro diagnostic kits for thyroid function testing, including the I-125 Anti-Thyroglobulin Antibody IRMA Test Kit, the I-125 Anti-Microsomal Antibody IRMA Test Kit, and the 125-I TSH Receptor Antibody Kit. These products are designed for radioimmunoassay (RIMA) and immunoradiometric assay (IRMA) applications to detect specific thyroid-related antibodies and receptors in patient samples.
The company’s diagnostic kits fall under FDA Class II devices and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) database. Cronus is based in the United States.
Catalogue
I-125 Anti-Thyroglobulin Antibody Irma Test Kit Ref K871193
510(k) 510(k)I-125 Anti-Microsomal Antibody Irma Test Kit Ref K871194
510(k) 510(k)125-I Tsh Receptor Antibody Kit Ref K863006
510(k) 510(k)
Frequently asked questions
How many devices does Cronus have in the registry?
The registry currently lists 3 devices for Cronus. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cronus's devices?
Among its 3 most recently registered devices, Cronus has devices listed in FDA 510(k) (3 devices).
What risk classes do Cronus's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cronus's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cronus in the registry?
The most recently registered devices listed for Cronus include I-125 ANTI-THYROGLOBULIN ANTIBODY IRMA TEST KIT, I-125 ANTI-MICROSOMAL ANTIBODY IRMA TEST KIT and 125-I TSH RECEPTOR ANTIBODY KIT.