Snapcpap
Country not established
- Devices
- 1
What Snapcpap makes
Snapcpap manufactures the DreamPort, a continuous positive airway pressure (CPAP) device designed for treating obstructive sleep apnea by delivering pressurized air to keep airways open during sleep.
The DreamPort is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Bleep DreamPort Ref K172335
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Snapcpap have in the registry?
The registry currently lists 1 device for Snapcpap. Devices recorded under merged duplicate company entries are counted once.
Which registries list Snapcpap's devices?
Among its 1 most recently registered device, Snapcpap has devices listed in FDA 510(k) (1 device).
What risk classes do Snapcpap's devices fall under?
Among its 1 most recently registered device, the classes recorded for Snapcpap's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Snapcpap in the registry?
The most recently registered devices listed for Snapcpap include Bleep DreamPort.