Medical Device Manufacturer · US , Poway , CA

Resmed Germany, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2006

Recent clearances: ApneaLink Air, APNEALINK PRO, STELLAR 150

View 8 510(k) Devices ↓

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Resmed Germany, Inc. Anesthesiology ✕

8 devices

1-8 of 8

Cleared Apr 30, 2015

Anesthesiology · 167d

Cleared Nov 08, 2013

Anesthesiology · 134d

Cleared Jun 17, 2013

Anesthesiology · 285d

Cleared Apr 05, 2012

Anesthesiology · 118d

Cleared Mar 01, 2011

Anesthesiology · 125d

Cleared Mar 19, 2009

APNEALINK PLUS, MODEL: 22328

Anesthesiology · 106d

Cleared Jun 15, 2007

Anesthesiology · 140d

Cleared Jul 25, 2006

APNEALINK, MODEL 22302

Anesthesiology · 67d