Peep Medical, LLC Dba Go2 Devices
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- Devices
- 1
What Peep Medical, LLC Dba Go2 Devices makes
Peep Medical, LLC (dba Go2 Devices) manufactures the Breathe+ device, a respiratory support system designed for noninvasive ventilation and continuous positive airway pressure (CPAP) therapy at home or in clinical settings.
The Breathe+ device 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
Breathe+ Ref K222018
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peep Medical, LLC Dba Go2 Devices have in the registry?
The registry currently lists 1 device for Peep Medical, LLC Dba Go2 Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peep Medical, LLC Dba Go2 Devices's devices?
Among its 1 most recently registered device, Peep Medical, LLC Dba Go2 Devices has devices listed in FDA 510(k) (1 device).
What risk classes do Peep Medical, LLC Dba Go2 Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for Peep Medical, LLC Dba Go2 Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peep Medical, LLC Dba Go2 Devices in the registry?
The most recently registered devices listed for Peep Medical, LLC Dba Go2 Devices include Breathe+.