• 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
-
21 to 30 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]
universal xacttrace MEDCARE FLAGA K043132 12/21/2004
ultima snoring mike, model 0540 BRAEBON MEDICAL CORP. K020312 08/07/2002
tempus pro patient monitor Remote Diagnostic Technologies Ltd. K173768 01/10/2018
tempus pro patient monitor Remote Diagnostic Technologies Limited K201746 09/18/2020
suzanne NELLCOR PURITAN BENNETT, INC. K990565 08/18/1999
stardust ii, model 1011176 RESPIRONICS, INC. K021845 05/20/2004
stardust ii RESPIRONICS, INC. K052573 12/13/2005
stardust RESPIRONICS, INC. K973920 05/14/1998
star 65 Skanray Technologies Pvt Ltd K172147 05/25/2018
spacelabs pathfinder sl holter analyzer SPACELABS HEALTHCARE LTD. K110001 06/14/2011
-
-