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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K120598
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PROCARE B40 Patient Monitor, V1; and B40 Patient Monitor, V2, V2.1, and V3. The PROCARE Monitor B... 2 12/07/2018 GE Healthcare, LLC
HGE Healthcare Patient Monitor B30, Procare Monitor B20, Procare Monitor B40, and Monitor B40 K1222... 2 12/12/2013 GE Healthcare, LLC
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