Saneso 镜头清洗瓶组件 (SAN-LWB-A)
K号: K222173 · 2023-02-27
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申请人Saneso, Inc.
决定日期2023-02-27
产品代码OCX
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
Saneso Lens Wash Bottle Assembly (SAN-LWB-A) is the device name listed in this FDA 510(k) record. The listed applicant is Saneso, Inc.. It received FDA 510(k) clearance on 2023-02-27 under 510(k) number K222173. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Saneso Lens Wash Bottle Assembly (SAN-LWB-A)?
Saneso Lens Wash Bottle Assembly (SAN-LWB-A) is a medical device that received FDA 510(k) clearance on 2023-02-27. The listed applicant is Saneso, Inc.. The 510(k) number is K222173.
When did Saneso Lens Wash Bottle Assembly (SAN-LWB-A) receive FDA 510(k) clearance?
Saneso Lens Wash Bottle Assembly (SAN-LWB-A) received FDA 510(k) clearance on 2023-02-27, under 510(k) number K222173.
Who is the listed applicant for Saneso Lens Wash Bottle Assembly (SAN-LWB-A)?
The FDA 510(k) record lists Saneso, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Saneso Lens Wash Bottle Assembly (SAN-LWB-A)?
The FDA product code for Saneso Lens Wash Bottle Assembly (SAN-LWB-A) is OCX.
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列明Saneso, Inc.为申报人的其他记录
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相关器械（代码：OCX）
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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