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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K832458
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FDA Recall
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ASP Automatic Endoscope Reprocessor (AER), Product Code: 20300 & 20301 The AER is a machine designe... 2 12/16/2010 FEI # 3003662624
Advanced Sterilization Products
ASP Automatic Endoscope Reprocessor, AER Plus Product Code 20300 and AER with printer Product Code ... 2 11/07/2008 FEI # 3003662624
Advanced Sterilization Products
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