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FDA 510(k)

Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup

K号: K250803 · 2025-04-15

申请人Anhui Deepblue Medical Technological Co., Ltd.
决定日期2025-04-15
产品代码NGL
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决定实质等同

器械摘要

Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Deepblue Medical Technological Co., Ltd.. It received FDA 510(k) clearance on 2025-04-15 under 510(k) number K250803. The device is classified under product code NGL. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup?

Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup is a medical device that received FDA 510(k) clearance on 2025-04-15. The listed applicant is Anhui Deepblue Medical Technological Co., Ltd.. The 510(k) number is K250803.

When did Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup receive FDA 510(k) clearance?

Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup received FDA 510(k) clearance on 2025-04-15, under 510(k) number K250803.

Who is the listed applicant for Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup?

The FDA 510(k) record lists Anhui Deepblue Medical Technological Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup?

The FDA product code for Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup is NGL.

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。

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相关器械（代码：NGL）

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

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