Merge Hemo，型号RCSV2
K号: K233326 · 2024-06-21
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决定日期2024-06-21
产品代码DQK
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
Merge Hemo, Model RCSV2 is the device name listed in this FDA 510(k) record. The listed applicant is Merge Healthcare Incorporated. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233326. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Merge Hemo, Model RCSV2?
Merge Hemo, Model RCSV2 is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Merge Healthcare Incorporated. The 510(k) number is K233326.
When did Merge Hemo, Model RCSV2 receive FDA 510(k) clearance?
Merge Hemo, Model RCSV2 received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233326.
Who is the listed applicant for Merge Hemo, Model RCSV2?
The FDA 510(k) record lists Merge Healthcare Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Merge Hemo, Model RCSV2?
The FDA product code for Merge Hemo, Model RCSV2 is DQK.
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Merge Healthcare Incorporated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：DQK）
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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