ResMed Corp - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
ResMed Corp has 15 FDA 510(k) cleared anesthesiology devices. Based in Poway, US.
Latest FDA clearance: Apr 2026. Active since 1997.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Apr 08, 2026
myAir
Anesthesiology
292d
Cleared
Dec 05, 2025
Personalized Therapy Comfort Settings (PTCS)
Anesthesiology
189d
Cleared
May 28, 2025
myAir
Anesthesiology
86d
Cleared
Sep 27, 2024
EasyCare Tx 2
Anesthesiology
87d
Cleared
Sep 26, 2024
myAir
Anesthesiology
148d
Cleared
Jan 17, 2021
Galapogos
Anesthesiology
319d
Cleared
May 12, 2014
S9 ELOUERA
Anesthesiology
116d
Cleared
May 25, 2012
VPAP ADAPT
Anesthesiology
155d
Cleared
Jun 30, 2011
S8 ASPEN WITH H4I PLUS
Anesthesiology
69d
Cleared
May 06, 2009
MIRAGE ECHO
Anesthesiology
70d
Cleared
Mar 10, 2004
S7 ELITE CPAP SYSTEM WITH SOMNOTRAXX SYSTEM
Anesthesiology
363d
Cleared
Jul 16, 2002
AUTOSET SPIRIT CPAP SYSTEM
Anesthesiology
238d
Cleared
Jul 08, 2002
S7 ELITE CP AP SYSTEM
Anesthesiology
224d
Cleared
Jun 24, 1998
SULLIVAN VPAP II ST-A NASAL VPAP SYSTEM
Anesthesiology
212d
Cleared
Sep 04, 1997
SULLIVAN HUMIDAIRE HEATED HUMIDIFIER
Anesthesiology
153d