Yoni.Fit 膀胱支持器
K号: K232525 · 2024-05-17
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决定日期2024-05-17
产品代码HHW
咨询委员会OB
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决定实质等同
器械摘要
Yoni.Fit Bladder Support is the device name listed in this FDA 510(k) record. The listed applicant is Watkins-Conti Products, Inc.. It received FDA 510(k) clearance on 2024-05-17 under 510(k) number K232525. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Yoni.Fit Bladder Support?
Yoni.Fit Bladder Support is a medical device that received FDA 510(k) clearance on 2024-05-17. The listed applicant is Watkins-Conti Products, Inc.. The 510(k) number is K232525.
When did Yoni.Fit Bladder Support receive FDA 510(k) clearance?
Yoni.Fit Bladder Support received FDA 510(k) clearance on 2024-05-17, under 510(k) number K232525.
Who is the listed applicant for Yoni.Fit Bladder Support?
The FDA 510(k) record lists Watkins-Conti Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Yoni.Fit Bladder Support?
The FDA product code for Yoni.Fit Bladder Support is HHW.
相关临床试验
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相关器械（代码：HHW）
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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