Medical Device Manufacturer · US , Poway , CA

ResMed Corp - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1997

Total

Cleared

Denied

ResMed Corp has 14 FDA 510(k) cleared anesthesiology devices. Based in Poway, US.

Latest FDA clearance: Dec 2025. 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.

FDA 510(k) cleared devices by ResMed Corp

14 devices

1-12 of 14

Cleared Dec 05, 2025

Personalized Therapy Comfort Settings (PTCS)

K251657 · BZD

Anesthesiology · 189d

Anesthesiology · 148d

Cleared Jan 17, 2021

Galapogos

K200565 · BZD

Anesthesiology · 319d

Cleared May 12, 2014

S9 ELOUERA

K140124 · BZD

Anesthesiology · 116d

Cleared May 25, 2012

VPAP ADAPT

K113801 · BZD

Anesthesiology · 155d

Cleared Jun 30, 2011

S8 ASPEN WITH H4I PLUS

S7 ELITE CPAP SYSTEM WITH SOMNOTRAXX SYSTEM

K030797 · BZD

Anesthesiology · 363d

Cleared Jul 16, 2002

AUTOSET SPIRIT CPAP SYSTEM

K013843 · BZD

Anesthesiology · 238d

Cleared Jul 08, 2002

S7 ELITE CP AP SYSTEM

K013909 · BZD

Anesthesiology · 224d

ResMed Corp - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by ResMed Corp

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