Medical Device Recalls
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1 result found
510(K) Number: K112213 |
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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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GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a gener... | 2 | 07/31/2013 | GE Healthcare, LLC |
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