• 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
-
1 to 10 of 24 Results
ProductCode: KDI Applicant: NXSTAGE MEDICAL, INC. Decision Date To: 05/05/2024
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 24 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]
versihd with guideme software NxStage Medical, Inc. K230632 08/11/2023
nxstage cartridge express with speedswap NxStage Medical, Inc. K183158 08/09/2019
nxstage system one NxStage Medical, Inc. K171331 08/24/2017
nxstage therapeutic plasma exchange (tpe) cartridge NxStage Medical, Inc. K143313 03/20/2015
nxstage system one NXSTAGE MEDICAL, INC. K140526 05/19/2014
nxstage system one with nxview NXSTAGE MEDICAL, INC. K133547 03/03/2014
streamline express NXSTAGE MEDICAL, INC. K132602 02/04/2014
nxstage 1.6m2 dialyzer NXSTAGE MEDICAL, INC. K131050 12/27/2013
nxstage system one NXSTAGE MEDICAL, INC. K122051 04/23/2013
nxstage system one low volume cartridge express NXSTAGE MEDICAL, INC. K123395 03/07/2013
-
-