Eko Model E5 System (EME5), Eko DUO
K号: K170874 · 2017-05-19
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决定日期2017-05-19
产品代码DQD
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
Eko Model E5 System (EME5), Eko DUO is the device name listed in this FDA 510(k) record. The listed applicant is Eko Devices, Inc.. It received FDA 510(k) clearance on 2017-05-19 under 510(k) number K170874. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Eko Model E5 System (EME5), Eko DUO?
Eko Model E5 System (EME5), Eko DUO is a medical device that received FDA 510(k) clearance on 2017-05-19. The listed applicant is Eko Devices, Inc.. The 510(k) number is K170874.
When did Eko Model E5 System (EME5), Eko DUO receive FDA 510(k) clearance?
Eko Model E5 System (EME5), Eko DUO received FDA 510(k) clearance on 2017-05-19, under 510(k) number K170874.
Who is the listed applicant for Eko Model E5 System (EME5), Eko DUO?
The FDA 510(k) record lists Eko Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eko Model E5 System (EME5), Eko DUO?
The FDA product code for Eko Model E5 System (EME5), Eko DUO is DQD.
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。
列明Eko Devices, Inc.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：DQD）
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。
K261494智能无线听诊器（STEMO310）；智能无线听诊器（STEMO710）；智能无线听诊器（STEMO720）；智能无线听诊器（STEMO730）Shanghai Hulu Devices Co., Ltd.K261694核心300数字听诊器Eko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089泰托听诊器（G3）Tyto Care , Ltd.K252076Kneevoice 软骨评估系统 (750-3600-001)Kneevoice, Inc.K252284eMurmur心脏AICsd Labs
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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