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FDA 510(k)

PM2系统及ECGuide连接器

K号: K240486 · 2024-09-08

决定日期2024-09-08
产品代码LJS
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

PM2 System and ECGuide Connector is the device name listed in this FDA 510(k) record. The listed applicant is Piccolo Medical, Inc.. It received FDA 510(k) clearance on 2024-09-08 under 510(k) number K240486. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PM2 System and ECGuide Connector?

PM2 System and ECGuide Connector is a medical device that received FDA 510(k) clearance on 2024-09-08. The listed applicant is Piccolo Medical, Inc.. The 510(k) number is K240486.

When did PM2 System and ECGuide Connector receive FDA 510(k) clearance?

PM2 System and ECGuide Connector received FDA 510(k) clearance on 2024-09-08, under 510(k) number K240486.

Who is the listed applicant for PM2 System and ECGuide Connector?

The FDA 510(k) record lists Piccolo Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PM2 System and ECGuide Connector?

The FDA product code for PM2 System and ECGuide Connector is LJS.

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Piccolo 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:LJS)

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

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