Immunotech S.A.
FranceFDA applicant, unverified
- Devices
- 1
What Immunotech S.A. makes
Immunotech S.A. manufactures the FT4 Radioimmunoassay, a diagnostic test used to measure free thyroxine (FT4) levels in blood samples, aiding in the assessment of thyroid function.
The FT4 Radioimmunoassay is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
FT4 Radioimmunoassay Ref K934012
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Immunotech S.A. have in the registry?
The registry currently lists 1 device for Immunotech S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Immunotech S.A.'s devices?
Among its 1 most recently registered device, Immunotech S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Immunotech S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Immunotech S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Immunotech S.A. in the registry?
The most recently registered devices listed for Immunotech S.A. include FT4 RADIOIMMUNOASSAY.