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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K011213
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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.
Synchron LX20 PRO, Part Number 476100, Beckman Coulter, Inc. 2 05/24/2008 FEI # 2050012
Beckman Coulter Inc
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
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