FDA 510(k)Foresight 心脏内超声心动图（ICE）系统
K号: K162789 · 2017-03-28
决定日期2017-03-28
产品代码DQO
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
Foresight Intracardiac Echocardiology (ICE) System is the device name listed in this FDA 510(k) record. The listed applicant is Conavi Medical, Inc.. It received FDA 510(k) clearance on 2017-03-28 under 510(k) number K162789. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Foresight Intracardiac Echocardiology (ICE) System?
Foresight Intracardiac Echocardiology (ICE) System is a medical device that received FDA 510(k) clearance on 2017-03-28. The listed applicant is Conavi Medical, Inc.. The 510(k) number is K162789.
When did Foresight Intracardiac Echocardiology (ICE) System receive FDA 510(k) clearance?
Foresight Intracardiac Echocardiology (ICE) System received FDA 510(k) clearance on 2017-03-28, under 510(k) number K162789.
Who is the listed applicant for Foresight Intracardiac Echocardiology (ICE) System?
The FDA 510(k) record lists Conavi Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Foresight Intracardiac Echocardiology (ICE) System?
The FDA product code for Foresight Intracardiac Echocardiology (ICE) System is DQO.
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Conavi Medical, 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：DQO）
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。
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