Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K200497 |
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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 Vivid S70N, ultrasound device | 2 | 07/10/2023 | GE Vingmed Ultrasound As |
GE Healthcare Vivid S60N, ultrasound device | 2 | 07/10/2023 | GE Vingmed Ultrasound As |
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