FDA 510(k)

Sensilift Pro (ST300XXYYZZZ)

K号: K250341 · 2026-01-06

决定日期2026-01-06

产品代码PAY

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决定实质等同

器械摘要

Sensilift Pro (ST300XXYYZZZ) is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2026-01-06 under 510(k) number K250341. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sensilift Pro (ST300XXYYZZZ)?

Sensilift Pro (ST300XXYYZZZ) is a medical device that received FDA 510(k) clearance on 2026-01-06. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K250341.

When did Sensilift Pro (ST300XXYYZZZ) receive FDA 510(k) clearance?

Sensilift Pro (ST300XXYYZZZ) received FDA 510(k) clearance on 2026-01-06, under 510(k) number K250341.

Who is the listed applicant for Sensilift Pro (ST300XXYYZZZ)?

The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sensilift Pro (ST300XXYYZZZ)?

The FDA product code for Sensilift Pro (ST300XXYYZZZ) is PAY.

列明El Global Trade, Ltd.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。

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