17HK700G-W
K号: K180332 · 2018-06-08
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器械摘要
17HK700G-W is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics. It received FDA 510(k) clearance on 2018-06-08 under 510(k) number K180332. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the 17HK700G-W?
17HK700G-W is a medical device that received FDA 510(k) clearance on 2018-06-08. The listed applicant is Lg Electronics. The 510(k) number is K180332.
When did 17HK700G-W receive FDA 510(k) clearance?
17HK700G-W received FDA 510(k) clearance on 2018-06-08, under 510(k) number K180332.
Who is the listed applicant for 17HK700G-W?
The FDA 510(k) record lists Lg Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 17HK700G-W?
The FDA product code for 17HK700G-W is MQB.
列明Lg Electronics为申报人的其他记录
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：MQB）
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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