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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K231328
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Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version ... 2 10/25/2024 FEI # 2124215
Boston Scientific Corporation
LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, ... 2 05/01/2026 FEI # 2124215
Boston Scientific Corporation
LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe)... 2 05/01/2026 FEI # 2124215
Boston Scientific Corporation
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