Withings BeamO (SCT02)
K号: K252474 · 2025-11-10
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器械摘要
Withings BeamO (SCT02) is the device name listed in this FDA 510(k) record. The listed applicant is Withings. It received FDA 510(k) clearance on 2025-11-10 under 510(k) number K252474. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Withings BeamO (SCT02)?
Withings BeamO (SCT02) is a medical device that received FDA 510(k) clearance on 2025-11-10. The listed applicant is Withings. The 510(k) number is K252474.
When did Withings BeamO (SCT02) receive FDA 510(k) clearance?
Withings BeamO (SCT02) received FDA 510(k) clearance on 2025-11-10, under 510(k) number K252474.
Who is the listed applicant for Withings BeamO (SCT02)?
The FDA 510(k) record lists Withings as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Withings BeamO (SCT02)?
The FDA product code for Withings BeamO (SCT02) is DPS.
相关临床试验
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列明Withings为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：DPS）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K254255S-Patch CardioAIWellysis Corp.K252463SE-1202系列心电图机（型号：SE-1202，SE-1202E）Edan Instruments, Inc.K251670MAC 7 静息心电图分析系统Ge Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K250569Cardiologs Holter PlatformPhilips France CommercialK243252ZBPro DiagnosticZbeats, Inc.
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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