Medical Device Recalls
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1 result found
510(K) Number: K072517 |
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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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iLab Ultrasound Imaging System, Models 120INS and 240INS, manufactured by Boston Scientific Corporat... | 2 | 09/23/2008 | Boston Scientific Corporation |
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