Medical Device Recalls
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1 result found
510(K) Number: K162743 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47... | 2 | 09/13/2024 | GE Healthcare GmbH |
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