Medical Device Recalls
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1 result found
510(K) Number: K063493 |
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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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| iReview" Software (Accessory To) iLab Ultrasound Imaging System, Model Number: H74900018010, Catal... | 2 | 09/17/2008 |
FEI # 2939204 Boston Scientific Corporation |
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