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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 of 167 Results
ProductCode: MNR Decision Date To: 09/26/2021
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Export all 167 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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menai system ResMed Ltd K160836 12/15/2016
apnealink plus, model: 22328 RESMED GERMANY INC. K083575 03/19/2009
apnealink pro RESMED GERMANY INC. K131932 11/08/2013
apnealink, model 22302 RESMED GERMANY INC. K061405 07/25/2006
apnealink air RESMED GERMANY INC. K143272 04/30/2015
apnealink RESMED GERMANY INC. K070263 06/15/2007
s9 elouera RESMED CORP K140124 05/12/2014
sleepcheckrx ResApp Health K213360 07/05/2022
tempus pro patient monitor Remote Diagnostic Technologies Ltd. K173768 01/10/2018
tempus pro patient monitor Remote Diagnostic Technologies Limited K201746 09/18/2020
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