Creme de La Femme Feminine Lubricant
K号: K180014 · 2018-12-21
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决定日期2018-12-21
产品代码NUC
咨询委员会OB
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器械摘要
Creme de La Femme Feminine Lubricant is the device name listed in this FDA 510(k) record. The listed applicant is Cewal, Inc. Dba Premiere Enterprises. It received FDA 510(k) clearance on 2018-12-21 under 510(k) number K180014. 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 Creme de La Femme Feminine Lubricant?
Creme de La Femme Feminine Lubricant is a medical device that received FDA 510(k) clearance on 2018-12-21. The listed applicant is Cewal, Inc. Dba Premiere Enterprises. The 510(k) number is K180014.
When did Creme de La Femme Feminine Lubricant receive FDA 510(k) clearance?
Creme de La Femme Feminine Lubricant received FDA 510(k) clearance on 2018-12-21, under 510(k) number K180014.
Who is the listed applicant for Creme de La Femme Feminine Lubricant?
The FDA 510(k) record lists Cewal, Inc. Dba Premiere Enterprises as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Creme de La Femme Feminine Lubricant?
The FDA product code for Creme de La Femme Feminine Lubricant 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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