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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K200621
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Version: 1.2.0 (1.2.0+85ela410) Caption Health, Caption AI, Ultrasound Imaging System Application So... 2 07/22/2021 Caption Health
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