K-D 平衡
K号: K173669 · 2018-04-02
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器械摘要
K-D Balance is the device name listed in this FDA 510(k) record. The listed applicant is King-Devick Technologies, Inc.. It received FDA 510(k) clearance on 2018-04-02 under 510(k) number K173669. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.
常见问题
What is the K-D Balance?
K-D Balance is a medical device that received FDA 510(k) clearance on 2018-04-02. The listed applicant is King-Devick Technologies, Inc.. The 510(k) number is K173669.
When did K-D Balance receive FDA 510(k) clearance?
K-D Balance received FDA 510(k) clearance on 2018-04-02, under 510(k) number K173669.
Who is the listed applicant for K-D Balance?
The FDA 510(k) record lists King-Devick Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for K-D Balance?
The FDA product code for K-D Balance is LXV.
相关临床试验
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相关器械（代码：LXV）
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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