Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
11 to 20 of 167 Results
ProductCode: MNR Decision Date To: 09/26/2021
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 167 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
apnea risk evaluation system (ares), model 620 Watermark Medical K160499 04/24/2017
vitascore VITASCORE B.V. K072014 11/08/2007
provent nasal cannula VENTUS MEDICAL, INC. K080983 08/07/2008
somnolyzer 24x7 THE SIESTA GROUP NORTH AMERICA K083620 03/06/2009
devilbiss sleep recorder model # rm60 SUNRISE MEDICAL HHG, INC. K012437 07/16/2002
spacelabs pathfinder sl holter analyzer SPACELABS HEALTHCARE LTD. K110001 06/14/2011
somnoscreen SOMNOMEDICS GMBH & CO. KG K060708 01/24/2007
somnotouch resp SOMNOMEDICS GMBH K140861 01/30/2015
somnowatch SOMNOMEDICS GMBH K081485 09/18/2008
somnoscreen plus Somnomedics GmbH K201054 08/12/2020
-
-