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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