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

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
1 to 4 of 4 Results
510(K) Number: K011213
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
SYNCHRON LX 20, SYNCHRON LX 20 PROClinical Systems; Operating Software Version 4.5; Part Number: A2... 3 05/25/2006 FEI # 2050012
Beckman Coulter Inc
Synchron LX20 PRO, Part Number 476100, Beckman Coulter, Inc. 2 05/24/2008 FEI # 2050012
Beckman Coulter Inc
Synchron LX20 PRO, Part Number: 476100. Designed for the in vitro determination of a variety of g... 1 05/06/2011 FEI # 2050012
Beckman Coulter Inc.
Synchron® LX 20 The Synchron LX Systems are fully automated, computer-controlled clinical chemis... 2 04/26/2011 FEI # 2050012
Beckman Coulter Inc.
-
-