FDA 510(k)

Grosz 加热液体，Grosz Play 刺激，Grosz KY Yours & Mine

K号: K213892 · 2023-03-07

决定日期2023-03-07

产品代码NUC

咨询委员会OB 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。

决定实质等同

器械摘要

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is the device name listed in this FDA 510(k) record. The listed applicant is Rb Health (Us), LLC. It received FDA 510(k) clearance on 2023-03-07 under 510(k) number K213892. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is a medical device that received FDA 510(k) clearance on 2023-03-07. The listed applicant is Rb Health (Us), LLC. The 510(k) number is K213892.

When did Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine receive FDA 510(k) clearance?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine received FDA 510(k) clearance on 2023-03-07, under 510(k) number K213892.

Who is the listed applicant for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

The FDA 510(k) record lists Rb Health (Us), LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

The FDA product code for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is NUC.

列明Rb Health (Us), LLC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。

K241617杜蕾斯聚异戊二烯避孕套 K230781Belle Sensilube K220489杜蕾斯帕特诺斯CloseFit，杜蕾斯帕特诺斯Regular K222068杜蕾斯Penck III Regular K211152Durex含苯佐卡因避孕套 K213647杜蕾斯帕特诺斯Wide

查看所有 14 个设备 →

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。