WHOOP 心电图（电生理图）功能（1.0）
K号: K243236 · 2025-04-04
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申请人Whoop., Inc.
决定日期2025-04-04
产品代码QDA
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
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产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
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请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同
器械摘要
WHOOP ECG (electrocardiogram) Feature (1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Whoop., Inc.. It received FDA 510(k) clearance on 2025-04-04 under 510(k) number K243236. The device is classified under product code QDA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the WHOOP ECG (electrocardiogram) Feature (1.0)?
WHOOP ECG (electrocardiogram) Feature (1.0) is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Whoop., Inc.. The 510(k) number is K243236.
When did WHOOP ECG (electrocardiogram) Feature (1.0) receive FDA 510(k) clearance?
WHOOP ECG (electrocardiogram) Feature (1.0) received FDA 510(k) clearance on 2025-04-04, under 510(k) number K243236.
Who is the listed applicant for WHOOP ECG (electrocardiogram) Feature (1.0)?
The FDA 510(k) record lists Whoop., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHOOP ECG (electrocardiogram) Feature (1.0)?
The FDA product code for WHOOP ECG (electrocardiogram) Feature (1.0) is QDA.
相关临床试验
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：QDA）
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。
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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