Thryotec
Country not established
- Devices
- 1
What Thryotec makes
Thryotec manufactures the THYRO TEST, a diagnostic device designed for thyroid function assessment, likely involving point-of-care or laboratory testing for thyroid hormone levels or markers.
The THYRO TEST 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
Thyro Test Ref K030912
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thryotec have in the registry?
The registry currently lists 1 device for Thryotec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thryotec's devices?
Among its 1 most recently registered device, Thryotec has devices listed in FDA 510(k) (1 device).
What risk classes do Thryotec's devices fall under?
Among its 1 most recently registered device, the classes recorded for Thryotec's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thryotec in the registry?
The most recently registered devices listed for Thryotec include THYRO TEST.