Medical Device Recalls
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1 result found
510(K) Number: K120201 |
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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 Vivid E9 ultrasound system. GE Vivid E9 is a Track 3 diagnostic ultrasound system, which is prim... | 2 | 11/21/2013 | GE Healthcare, LLC |
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