SiOxD 创面基质
K号: K232847 · 2023-12-18
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器械摘要
SiOxD Wound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Sioxmed, LLC. It received FDA 510(k) clearance on 2023-12-18 under 510(k) number K232847. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.
常见问题
What is the SiOxD Wound Matrix?
SiOxD Wound Matrix is a medical device that received FDA 510(k) clearance on 2023-12-18. The listed applicant is Sioxmed, LLC. The 510(k) number is K232847.
When did SiOxD Wound Matrix receive FDA 510(k) clearance?
SiOxD Wound Matrix received FDA 510(k) clearance on 2023-12-18, under 510(k) number K232847.
Who is the listed applicant for SiOxD Wound Matrix?
The FDA 510(k) record lists Sioxmed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SiOxD Wound Matrix?
The FDA product code for SiOxD Wound Matrix is QSZ.
相关临床试验
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列明Sioxmed, LLC为申报人的其他记录
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相关器械（代码：QSZ）
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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