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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K182417
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ROSA One 3.1 Brain Application 2 02/11/2020 FEI # 3009185973
MEDTECH SAS
ROSA Brain 3.0 Application-Brain 2 02/11/2020 FEI # 3009185973
MEDTECH SAS
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