Snorer's Friend
K号: K171529 · 2018-01-02
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决定日期2018-01-02
产品代码LRK
咨询委员会DE
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器械摘要
Snorer's Friend is the device name listed in this FDA 510(k) record. The listed applicant is Scope Healthcare Technologies Pty, Ltd.. It received FDA 510(k) clearance on 2018-01-02 under 510(k) number K171529. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Snorer's Friend?
Snorer's Friend is a medical device that received FDA 510(k) clearance on 2018-01-02. The listed applicant is Scope Healthcare Technologies Pty, Ltd.. The 510(k) number is K171529.
When did Snorer's Friend receive FDA 510(k) clearance?
Snorer's Friend received FDA 510(k) clearance on 2018-01-02, under 510(k) number K171529.
Who is the listed applicant for Snorer's Friend?
The FDA 510(k) record lists Scope Healthcare Technologies Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Snorer's Friend?
The FDA product code for Snorer's Friend is LRK.
相关临床试验
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相关器械（代码：LRK）
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。
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