Medical Device Recalls
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1 result found
510(K) Number: K143530 |
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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, Aespire 7900, 1009-9012-000 & Aespire View, 1009-9212-000. The family of GE Datex-... | 2 | 01/21/2016 | GE Medical Systems, LLC |
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