Dermatrix Duo
K号: K251836 · 2026-02-06
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决定日期2026-02-06
产品代码GEI
咨询委员会SU
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器械摘要
Dermatrix Duo is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Gsd Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K251836. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Dermatrix Duo?
Dermatrix Duo is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Shenzhen Gsd Technology Co., Ltd.. The 510(k) number is K251836.
When did Dermatrix Duo receive FDA 510(k) clearance?
Dermatrix Duo received FDA 510(k) clearance on 2026-02-06, under 510(k) number K251836.
Who is the listed applicant for Dermatrix Duo?
The FDA 510(k) record lists Shenzhen Gsd Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dermatrix Duo?
The FDA product code for Dermatrix Duo is GEI.
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。
相关器械（代码：GEI）
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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