外科手术服
K号: K213844 · 2023-02-16
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决定日期2023-02-16
产品代码FYA
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Surgical Gown is the device name listed in this FDA 510(k) record. The listed applicant is Bayteks Teknik Tekstil San. VE Tic. A.S.. It received FDA 510(k) clearance on 2023-02-16 under 510(k) number K213844. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Surgical Gown?
Surgical Gown is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Bayteks Teknik Tekstil San. VE Tic. A.S.. The 510(k) number is K213844.
When did Surgical Gown receive FDA 510(k) clearance?
Surgical Gown received FDA 510(k) clearance on 2023-02-16, under 510(k) number K213844.
Who is the listed applicant for Surgical Gown?
The FDA 510(k) record lists Bayteks Teknik Tekstil San. VE Tic. A.S. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Surgical Gown?
The FDA product code for Surgical Gown is FYA.
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：FYA）
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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