SCOUT MD 外科引导系统
K号: K231468 · 2024-02-12
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决定日期2024-02-12
产品代码NEU
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
SCOUT MD Surgical Guidance System is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical System, Inc.. It received FDA 510(k) clearance on 2024-02-12 under 510(k) number K231468. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SCOUT MD Surgical Guidance System?
SCOUT MD Surgical Guidance System is a medical device that received FDA 510(k) clearance on 2024-02-12. The listed applicant is Merit Medical System, Inc.. The 510(k) number is K231468.
When did SCOUT MD Surgical Guidance System receive FDA 510(k) clearance?
SCOUT MD Surgical Guidance System received FDA 510(k) clearance on 2024-02-12, under 510(k) number K231468.
Who is the listed applicant for SCOUT MD Surgical Guidance System?
The FDA 510(k) record lists Merit Medical System, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCOUT MD Surgical Guidance System?
The FDA product code for SCOUT MD Surgical Guidance System is NEU.
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Merit Medical System, 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：NEU）
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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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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