Medical Device Recalls
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1 result found
510(K) Number: K831756 |
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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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| Anspach BlackMax Pneumatic Motor System; ENT Surgical Drill, including handpiece and Accessories Att... | 2 | 02/13/2008 | The Anspach Effort, Inc. |
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