VagiVital Aktivgel
K号: K200098 · 2020-11-10
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决定日期2020-11-10
产品代码NUC
咨询委员会OB
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器械摘要
VagiVital Aktivgel is the device name listed in this FDA 510(k) record. The listed applicant is Peptonic Medical AB. It received FDA 510(k) clearance on 2020-11-10 under 510(k) number K200098. 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 VagiVital Aktivgel?
VagiVital Aktivgel is a medical device that received FDA 510(k) clearance on 2020-11-10. The listed applicant is Peptonic Medical AB. The 510(k) number is K200098.
When did VagiVital Aktivgel receive FDA 510(k) clearance?
VagiVital Aktivgel received FDA 510(k) clearance on 2020-11-10, under 510(k) number K200098.
Who is the listed applicant for VagiVital Aktivgel?
The FDA 510(k) record lists Peptonic Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VagiVital Aktivgel?
The FDA product code for VagiVital Aktivgel is NUC.
相关临床试验
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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。
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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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