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FDA 510(k) Applications Submitted by RESMED LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160836
03/25/2016
Menai System
ResMed Ltd
K160822
03/24/2016
S9 VPAP Adapt, VPAP Adapt, AirCurve 10 ASV
RESMED LTD
K161487
05/31/2016
VPAP Adapt SV, VPAP Tx, S9 VPAP Tx
ResMed Ltd
K161492
06/01/2016
Juno VPAP ST-A
ResMed Ltd
K153061
10/21/2015
Juno VPAP ST-A
RESMED LTD
K140054
01/09/2014
RESCAN
RESMED LTD
K170924
03/29/2017
AirFit F20
ResMed Ltd
K180497
02/26/2018
Scone Mask
ResMed Ltd
K171212
04/25/2017
AirFit N20
ResMed Ltd
K161978
07/18/2016
AirFit N20
ResMed Ltd
K153673
12/21/2015
AirFit N20
ResMed Ltd
K183512
12/18/2018
Moore Park Mask
ResMed Ltd
K172875
09/21/2017
Astral 100/150
ResMed Ltd
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