Khi, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Khi, Inc. makes
Khi, Inc. manufactures respiratory support devices, including breathing circuits for critical care, emergency resuscitators with aspiration capabilities, and specialized valves and couplings for medical gas delivery systems.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Khi Cpram Breathing Circuit Ref K811858
Regimes: 510(k) Registry: 510(k)Emergiency Resuscitator/Inhalor W/Aspir. Ref K800456
Regimes: 510(k) Registry: 510(k)Rad Valve Ref K830404
Regimes: 510(k) Registry: 510(k)Coupling/Valve Ref K830399
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Khi, Inc. have in the registry?
The registry currently lists 4 devices for Khi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Khi, Inc.'s devices?
Among its 4 most recently registered devices, Khi, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Khi, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Khi, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Khi, Inc. in the registry?
The most recently registered devices listed for Khi, Inc. include KHI CPRAM BREATHING CIRCUIT, EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR., RAD VALVE and COUPLING/VALVE.