Medical Device Recalls
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1 result found
510(K) Number: K961310 |
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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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| Bausch & Lomb Millennium Microsurgical System. | 2 | 05/26/2010 |
FEI # 1317628 Bausch & Lomb Inc |
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