Huestis Medical
Country not established
- Devices
- 1
What Huestis Medical makes
Huestis Medical manufactures the OSIRIS, a medical device designed for use in specific diagnostic or procedural applications within radiology or interventional radiology, such as contrast-enhanced imaging or catheter-based interventions.
The OSIRIS device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Osiris Ref K981153
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Huestis Medical have in the registry?
The registry currently lists 1 device for Huestis Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huestis Medical's devices?
Among its 1 most recently registered device, Huestis Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Huestis Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Huestis Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Huestis Medical in the registry?
The most recently registered devices listed for Huestis Medical include OSIRIS.