Medical Device Recalls
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1 result found
510(K) Number: K033139 |
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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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Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139, K061525, K082374, K092140... | 2 | 12/22/2022 | GE Medical Systems, LLC |
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