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 68 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORP Decision Date To: 10/22/2016
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
Results per Page
New Search  
Export all 68 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]
check valve BAXTER HEALTHCARE CORP. K881052 05/26/1988
clearlink antimicrobial luer activated device (lad) and extension sets with the clearlink antimicrobial luer activated BAXTER HEALTHCARE CORP. K072576 11/06/2007
colleague pump syringe adapter set BAXTER HEALTHCARE CORP. K982672 09/04/1998
continu-flo solution set BAXTER HEALTHCARE CORP. K971701 06/06/1997
continu-flo(r) solution set BAXTER HEALTHCARE CORP. K921703 06/04/1992
continuflo solution set/secondary medication set BAXTER HEALTHCARE CORP. K961225 06/21/1996
control-a-flo(tm) regulator BAXTER HEALTHCARE CORP. K940867 05/05/1994
dual luer lock cap BAXTER HEALTHCARE CORP. K981318 04/22/1998
dual luer lock cap, model 2c6250 BAXTER HEALTHCARE CORP. K101385 06/22/2010
extended life injection site BAXTER HEALTHCARE CORP. K882007 06/20/1988
-
-