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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K062024
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Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO m... 2 11/20/2012 FEI # 2517506
Siemens Healthcare Diagnostics, Inc.
Dimension Vista(R) Gentamicin (GENT) Flex(R) reagent cartridge, K4012 This method is an in vitro di... 2 03/21/2011 FEI # 2517506
Siemens Healthcare Diagnostics, Inc.
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