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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K981054
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Cidex Plus Solution Test Strips 3 03/29/2003 FEI # 3003662624
Advanced Sterilization Products
Cidexplus Solution Test Strips 2 04/27/2005 FEI # 3003662624
Advanced Sterilization Products
Gluteraldehyde Concentration Indicators ''Browne GA Indicator for CIDEX PLUS Products'' 3 09/21/2004 FEI # 3003662624
Advanced Sterilization Products
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