免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

The Sex Gel

K号: K181078 · 2018-09-10

决定日期2018-09-10
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

The Sex Gel is the device name listed in this FDA 510(k) record. The listed applicant is Necessaire, Inc.. It received FDA 510(k) clearance on 2018-09-10 under 510(k) number K181078. 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 The Sex Gel?

The Sex Gel is a medical device that received FDA 510(k) clearance on 2018-09-10. The listed applicant is Necessaire, Inc.. The 510(k) number is K181078.

When did The Sex Gel receive FDA 510(k) clearance?

The Sex Gel received FDA 510(k) clearance on 2018-09-10, under 510(k) number K181078.

Who is the listed applicant for The Sex Gel?

The FDA 510(k) record lists Necessaire, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for The Sex Gel?

The FDA product code for The Sex Gel is NUC.

相关器械(代码:NUC)

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。

↑