Hospicon Products
United KingdomFDA applicant, unverified
- Devices
- 1
What Hospicon Products makes
Hospicon Products manufactures the CLINIJEL, a medical device designed for wound care or skin preparation in clinical settings.
The CLINIJEL is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Clinijel Ref K970581
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hospicon Products have in the registry?
The registry currently lists 1 device for Hospicon Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hospicon Products's devices?
Among its 1 most recently registered device, Hospicon Products has devices listed in FDA 510(k) (1 device).
What risk classes do Hospicon Products's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hospicon Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hospicon Products in the registry?
The most recently registered devices listed for Hospicon Products include CLINIJEL.