S-Patch (S-Patch ExL)
K号: K233906 · 2024-02-16
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器械摘要
S-Patch (S-Patch ExL) is the device name listed in this FDA 510(k) record. The listed applicant is Wellysis Corp.. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K233906. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the S-Patch (S-Patch ExL)?
S-Patch (S-Patch ExL) is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Wellysis Corp.. The 510(k) number is K233906.
When did S-Patch (S-Patch ExL) receive FDA 510(k) clearance?
S-Patch (S-Patch ExL) received FDA 510(k) clearance on 2024-02-16, under 510(k) number K233906.
Who is the listed applicant for S-Patch (S-Patch ExL)?
The FDA 510(k) record lists Wellysis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S-Patch (S-Patch ExL)?
The FDA product code for S-Patch (S-Patch ExL) is DSH.
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。
列明Wellysis Corp.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。
相关器械（代码：DSH）
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
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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