Consumer Health Products, Inc.
Country not established
- Devices
- 1
What Consumer Health Products, Inc. makes
Consumer Health Products, Inc. manufactures the SNORERX 9.0, a Class II medical device.
The SNORERX 9.0 is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Snorerx 9.0 Ref K112205
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Consumer Health Products, Inc. have in the registry?
The registry currently lists 1 device for Consumer Health Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Consumer Health Products, Inc.'s devices?
Among its 1 most recently registered device, Consumer Health Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Consumer Health Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Consumer Health Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Consumer Health Products, Inc. in the registry?
The most recently registered devices listed for Consumer Health Products, Inc. include SNORERX 9.0.