Honda 步行辅助装置
K号: K181294 · 2018-12-14
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决定日期2018-12-14
产品代码PHL
咨询委员会PM
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决定实质等同
器械摘要
Honda Walking Assist Device is the device name listed in this FDA 510(k) record. The listed applicant is Honda Motor Company, Ltd.. It received FDA 510(k) clearance on 2018-12-14 under 510(k) number K181294. The device is classified under product code PHL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Honda Walking Assist Device?
Honda Walking Assist Device is a medical device that received FDA 510(k) clearance on 2018-12-14. The listed applicant is Honda Motor Company, Ltd.. The 510(k) number is K181294.
When did Honda Walking Assist Device receive FDA 510(k) clearance?
Honda Walking Assist Device received FDA 510(k) clearance on 2018-12-14, under 510(k) number K181294.
Who is the listed applicant for Honda Walking Assist Device?
The FDA 510(k) record lists Honda Motor Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Honda Walking Assist Device?
The FDA product code for Honda Walking Assist Device is PHL.
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：PHL）
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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