FDA 510(k)

Modular Medical MODD1 胰岛素输送系统

K号: K240158 · 2024-09-04

决定日期2024-09-04

产品代码LZG

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

Modular Medical MODD1 Insulin Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Modular Medical, Inc.. It received FDA 510(k) clearance on 2024-09-04 under 510(k) number K240158. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Modular Medical MODD1 Insulin Delivery System?

Modular Medical MODD1 Insulin Delivery System is a medical device that received FDA 510(k) clearance on 2024-09-04. The listed applicant is Modular Medical, Inc.. The 510(k) number is K240158.

When did Modular Medical MODD1 Insulin Delivery System receive FDA 510(k) clearance?

Modular Medical MODD1 Insulin Delivery System received FDA 510(k) clearance on 2024-09-04, under 510(k) number K240158.

Who is the listed applicant for Modular Medical MODD1 Insulin Delivery System?

FDA 510(k)记录中列出了Modular Medical, Inc.为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Modular Medical MODD1 Insulin Delivery System?

The FDA product code for Modular Medical MODD1 Insulin Delivery System is LZG.

列明Modular 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。

K262153Pivot 胰岛素输送系统

官方来源

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