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
-
61 to 68 of 68 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORP Decision Date To: 09/26/2016
 < 
 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]
solution administration sets with capless luer activated valve BAXTER HEALTHCARE CORP. K003225 10/19/2000
solution administration with luer access injection site BAXTER HEALTHCARE CORP. K042936 11/26/2004
solution set with 1.2 micron air eliminating filter BAXTER HEALTHCARE CORP. K952074 07/27/1995
sub-q-set(r) subcutaneous infusion set BAXTER HEALTHCARE CORP. K925362 08/28/1993
v-link antimicrobial luer activated device and extension sets with v-link antimicrobial luer activated device BAXTER HEALTHCARE CORP. K081289 08/04/2008
volumetric pump solution set for flo-gard 8000 BAXTER HEALTHCARE CORP. K893716 09/18/1989
volumetric pump solution set modified cassette BAXTER HEALTHCARE CORP. K912141 09/11/1991
volumetric pump solution set w/integral airway BAXTER HEALTHCARE CORP. K893646 12/06/1989
-
-