Sands Hyperbarics
Country not established
- Devices
- 1
What Sands Hyperbarics makes
Sands Hyperbarics manufactures hyperbaric chambers, including the Sands Series III model, designed for medical oxygen therapy under increased atmospheric pressure. These devices are primarily used in clinical settings for treating conditions such as decompression sickness, carbon monoxide poisoning, and wound healing.
The company’s hyperbaric chambers fall under FDA Class II devices and are subject to 510(k) clearance requirements in the United States. The portfolio is regulated under US medical device laws, with listings maintained through the FDA’s 510(k) pathway.
Catalogue
Sands Series Iii Hyperbaric Chamber Ref K972908
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sands Hyperbarics have in the registry?
The registry currently lists 1 device for Sands Hyperbarics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sands Hyperbarics's devices?
Among its 1 most recently registered device, Sands Hyperbarics has devices listed in FDA 510(k) (1 device).
What risk classes do Sands Hyperbarics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sands Hyperbarics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sands Hyperbarics in the registry?
The most recently registered devices listed for Sands Hyperbarics include SANDS SERIES III HYPERBARIC CHAMBER.