Hypnocore, Ltd.
Country not established
- Devices
- 1
What Hypnocore, Ltd. makes
Hypnocore, Ltd. makes the HC1000P Sleep Diagnosis Software System, a software-based medical device used for sleep diagnosis.
The HC1000P Sleep Diagnosis Software System is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
HC1000P Sleep Diagnosis Software System Ref K073269
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hypnocore, Ltd. have in the registry?
The registry currently lists 1 device for Hypnocore, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hypnocore, Ltd.'s devices?
Among its 1 most recently registered device, Hypnocore, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hypnocore, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hypnocore, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hypnocore, Ltd. in the registry?
The most recently registered devices listed for Hypnocore, Ltd. include HC1000P SLEEP DIAGNOSIS SOFTWARE SYSTEM.