By DrBicuspid Staff

January 11, 2017 -- Medical device company ResMed has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its AirMini portable continuous positive airway pressure (CPAP) device.

The AirMini is a small, fully featured CPAP device designed to be a user's secondary device, used such as when traveling. The product is not yet commercially available but will launched later in 2017, according to the company.

Copyright © 2017

To read this and get access to all of the exclusive content on create a free account or sign-in now.

Member Sign In:
MemberID or email address:  
Do you have a password?
No, I want a free membership.
Yes, I have a password:  
Forgot your password?
Sign in using your social networking account:
Sign in using your social networking