Resmed Germany, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K143272ApneaLink AirApril 30, 2015
K131932APNEALINK PRONovember 8, 2013
K122715STELLAR 150June 17, 2013
K113640STELLAR 150April 5, 2012
K103167STELLAR 150March 1, 2011
K083575APNEALINK PLUS, MODEL: 22328March 19, 2009
K070263APNEALINKJune 15, 2007
K061405APNEALINK, MODEL 22302July 25, 2006