SYLK PERSONAL LUBRICANT
K号: K152646 · 2016-03-11
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决定日期2016-03-11
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
SYLK PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Toro Management, LLC Dba Sylk. It received FDA 510(k) clearance on 2016-03-11 under 510(k) number K152646. 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 SYLK PERSONAL LUBRICANT?
SYLK PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2016-03-11. The listed applicant is Toro Management, LLC Dba Sylk. The 510(k) number is K152646.
When did SYLK PERSONAL LUBRICANT receive FDA 510(k) clearance?
SYLK PERSONAL LUBRICANT received FDA 510(k) clearance on 2016-03-11, under 510(k) number K152646.
Who is the listed applicant for SYLK PERSONAL LUBRICANT?
The FDA 510(k) record lists Toro Management, LLC Dba Sylk as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYLK PERSONAL LUBRICANT?
The FDA product code for SYLK PERSONAL 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
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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