Medical Device Recalls
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1 result found
510(K) Number: K082374 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vivid q ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN;... | 2 | 12/22/2022 |
FEI # 2126677 GE Medical Systems, LLC |
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