FDA 510(k) Applications Submitted by RESMED GERMANY INC.

FDA 510(k) Number Submission Date Device Name Applicant
K070263 01/26/2007 APNEALINK RESMED GERMANY INC.
K061405 05/19/2006 APNEALINK, MODEL 22302 RESMED GERMANY INC.
K083575 12/03/2008 APNEALINK PLUS, MODEL: 22328 RESMED GERMANY INC.
K113640 12/09/2011 STELLAR 150 RESMED GERMANY INC.
K122715 09/05/2012 STELLAR 150 RESMED GERMANY INC.
K131932 06/27/2013 APNEALINK PRO RESMED GERMANY INC.
K103167 10/27/2010 STELLAR 150 RESMED GERMANY INC.
K143272 11/14/2014 ApneaLink Air RESMED GERMANY INC.


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