Resitu 滑动器 09 (RESL09)
K号: K252183 · 2025-09-24
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决定日期2025-09-24
产品代码KNW
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
Resitu Slider 09 (RESL09) is the device name listed in this FDA 510(k) record. The listed applicant is Resitu Medical AB. It received FDA 510(k) clearance on 2025-09-24 under 510(k) number K252183. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Resitu Slider 09 (RESL09)?
Resitu Slider 09 (RESL09) is a medical device that received FDA 510(k) clearance on 2025-09-24. The listed applicant is Resitu Medical AB. The 510(k) number is K252183.
When did Resitu Slider 09 (RESL09) receive FDA 510(k) clearance?
Resitu Slider 09 (RESL09) received FDA 510(k) clearance on 2025-09-24, under 510(k) number K252183.
Who is the listed applicant for Resitu Slider 09 (RESL09)?
The FDA 510(k) record lists Resitu Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Resitu Slider 09 (RESL09)?
The FDA product code for Resitu Slider 09 (RESL09) is KNW.
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：KNW）
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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