ClearanceBrief
Company ยท US

Resmed Germany, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2015. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MNRVentilatory Effort Recorder5
MNTContinuous, Minimal Ventilatory Support, Facility Use Ventilator3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 30, 2015K143272ApneaLink Air
Resmed Germany, Inc., DE
MNR
Nov 8, 2013K131932APNEALINK PRO
Resmed Germany, Inc., DE
MNR
Jun 17, 2013K122715STELLAR 150
Resmed Germany, Inc.
MNT
Apr 5, 2012K113640STELLAR 150
Resmed Germany, Inc.
MNT
Mar 1, 2011K103167STELLAR 150
Resmed Germany, Inc., DE
MNT
Mar 19, 2009K083575APNEALINK PLUS, MODEL: 22328
Resmed Germany, Inc.
MNR
Jun 15, 2007K070263APNEALINK
Resmed Germany, Inc.
MNR
Jul 25, 2006K061405APNEALINK, MODEL 22302
Resmed Germany, Inc.
MNR

Latest recalls

DateFirm and productCodeLinked 510(k)
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