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
K172875 09/21/2017 Astral 100/150 ResMed Ltd


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