沃蒂亚™
K号: K173808 · 2018-07-27
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器械摘要
Voutia™ is the device name listed in this FDA 510(k) record. The listed applicant is Jeffrey Ward Cash, Dds. It received FDA 510(k) clearance on 2018-07-27 under 510(k) number K173808. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常见问题
What is the Voutia™?
Voutia™ is a medical device that received FDA 510(k) clearance on 2018-07-27. The listed applicant is Jeffrey Ward Cash, Dds. The 510(k) number is K173808.
When did Voutia™ receive FDA 510(k) clearance?
Voutia™ received FDA 510(k) clearance on 2018-07-27, under 510(k) number K173808.
Who is the listed applicant for Voutia™?
The FDA 510(k) record lists Jeffrey Ward Cash, Dds as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Voutia™?
The FDA product code for Voutia™ is LFD.
相关临床试验
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。
相关器械（代码：LFD）
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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