Clinical Immuno-Diagnostics
Country not established
- Devices
- 2
What Clinical Immuno-Diagnostics makes
Clinical Immuno-Diagnostics manufactures diagnostic tests for thyroid function, including a radioimmunoassay (RIA) for serum thyroxine and a thyroid indicator using radioactive iodine (¹²⁵I). These products are designed for laboratory use to measure hormone levels in patient samples.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Thyro-Indicator T-3 125I Ref K780018
Regimes: 510(k) Registry: 510(k)Ria For Serum Thyroxine Ref K771415
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Immuno-Diagnostics have in the registry?
The registry currently lists 2 devices for Clinical Immuno-Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Immuno-Diagnostics's devices?
Among its 2 most recently registered devices, Clinical Immuno-Diagnostics has devices listed in FDA 510(k) (2 devices).
What risk classes do Clinical Immuno-Diagnostics's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clinical Immuno-Diagnostics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Immuno-Diagnostics in the registry?
The most recently registered devices listed for Clinical Immuno-Diagnostics include THYRO-INDICATOR T-3 125I and RIA FOR SERUM THYROXINE.