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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: K130773
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Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00... 2 04/24/2025 FEI # 3003832357
Remote Diagnostic Technologies Ltd.
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