Medical Device Recalls
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1 result found
510(K) Number: K931049 |
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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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Monitor suspensions used with Advantx Legacy, RFX Classical, SFX-90, Model # 46-240838G2, manufactur... | 2 | 10/27/2008 | GE Healthcare |
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