Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K832458 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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