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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: K142398
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Recall
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Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green L... 2 06/27/2023 FEI # 3002806902
Ellex Medical Pty Ltd.
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