Medical Device Recalls
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1 result found
510(K) Number: K990793 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AccuGuide Injection Needles (Surface electrodes) The AccuGuide EMG Injection Needle, product 82... | 3 | 03/07/2007 | Medtronic Xomed, Inc. |
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