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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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