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FDA 510(k)

L-Cath™ 单双腔导管,L-Cath™ 中线导管

K号: K230669 · 2023-11-30

决定日期2023-11-30
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

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices. It received FDA 510(k) clearance on 2023-11-30 under 510(k) number K230669. 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 L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is a medical device that received FDA 510(k) clearance on 2023-11-30. The listed applicant is Argon Medical Devices. The 510(k) number is K230669.

When did L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters receive FDA 510(k) clearance?

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters received FDA 510(k) clearance on 2023-11-30, under 510(k) number K230669.

Who is the listed applicant for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

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

What is the FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

The FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters 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Argon Medical Devices为申报人的其他记录

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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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