Medical Device Recalls
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1 result found
510(K) Number: K971083 |
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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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| EBI VueCath Endoscopic Spinal System | 2 | 07/15/2003 |
FEI # 2242816 EBI, L.P. |
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