The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 09, 2019

Filed:

Jun. 06, 2014
Applicant:

Resmed Pty Ltd, Bella Vista, New South Wales, AU;

Inventors:

Philip Rodney Kwok, Sydney, AU;

Ron Richard, Escondido, CA (US);

Karthikeyan Selvarajan, Sydney, AU;

Glenn Richards, Auckland, NZ;

Nicholas Jerome Reed, Sydney, AU;

Larry Puckeridge, Sydney, AU;

Assignee:

ResMed Pty Ltd, Bella Vista, AU;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61M 16/00 (2006.01); A61B 5/0476 (2006.01); A61B 5/087 (2006.01); A61B 5/00 (2006.01); A61M 16/06 (2006.01); A61M 16/08 (2006.01);
U.S. Cl.
CPC ...
A61M 16/0069 (2014.02); A61B 5/0476 (2013.01); A61B 5/087 (2013.01); A61B 5/4812 (2013.01); A61B 5/4818 (2013.01); A61B 5/4836 (2013.01); A61M 16/0003 (2014.02); A61M 16/0051 (2013.01); A61M 16/0666 (2013.01); A61M 16/0875 (2013.01); A61M 16/06 (2013.01); A61M 16/0605 (2014.02); A61M 2016/0021 (2013.01); A61M 2016/0027 (2013.01); A61M 2016/0036 (2013.01); A61M 2205/13 (2013.01); A61M 2205/15 (2013.01); A61M 2205/502 (2013.01); A61M 2205/52 (2013.01);
Abstract

A method of operating a device for treating sleep disordered breathing (SDB), wherein the device provides continuous positive airway pressure during sleep, includes determining whether treatment pressure at the patient interface is below a desired value, in response to the determining, increasing pressure generated by the flow generator, in response to the increasing, making a determination that the increase in flow generator pressure has resulted in less than a desired increase in treatment pressure at the patient interface, and in response to the determination, reducing or inhibiting further increase of the flow generator pressure.


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