Satisfaite
K号: K190752 · 2019-12-13
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决定日期2019-12-13
产品代码NUC
咨询委员会OB
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决定实质等同
器械摘要
Satisfaite is the device name listed in this FDA 510(k) record. The listed applicant is Femmepharma Consumer Healthcare, LLC. It received FDA 510(k) clearance on 2019-12-13 under 510(k) number K190752. 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 Satisfaite?
Satisfaite is a medical device that received FDA 510(k) clearance on 2019-12-13. The listed applicant is Femmepharma Consumer Healthcare, LLC. The 510(k) number is K190752.
When did Satisfaite receive FDA 510(k) clearance?
Satisfaite received FDA 510(k) clearance on 2019-12-13, under 510(k) number K190752.
Who is the listed applicant for Satisfaite?
The FDA 510(k) record lists Femmepharma Consumer Healthcare, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Satisfaite?
The FDA product code for Satisfaite 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
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