Medical Device Recalls
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1 result found
510(K) Number: K152993 |
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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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MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, ... | 2 | 04/13/2022 | GE Healthcare, LLC |
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