Medical Device Recalls
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1 result found
510(K) Number: K122114 |
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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 LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) and LOGIQ S7 (with software revis... | 2 | 04/11/2013 | GE Healthcare, LLC |
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