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FDA 510(k) Applications Submitted by RESMED CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090490
02/25/2009
MIRAGE ECHO
RESMED CORP.
K030797
03/13/2003
S7 ELITE CPAP SYSTEM WITH SOMNOTRAXX SYSTEM; AUTOSET SPIRIT CPAP SYSTEM WITH SOMNOTRAXX SYSTEM
RESMED CORP.
K111148
04/22/2011
S8 ASPEN WITH H4I PLUS
RESMED CORP.
K971260
04/04/1997
SULLIVAN HUMIDAIRE HEATED HUMIDIFIER
RESMED CORP.
K013843
11/20/2001
AUTOSET SPIRIT CPAP SYSTEM
RESMED CORP.
K013909
11/26/2001
S7 ELITE CP AP SYSTEM
RESMED CORP.
K974417
11/24/1997
SULLIVAN VPAP II ST-A NASAL VPAP SYSTEM
RESMED CORP.
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