8通道膝关节-足部SPEEDER
K号: K162946 · 2017-01-06
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器械摘要
8ch Knee-Foot SPEEDER is the device name listed in this FDA 510(k) record. The listed applicant is Quality Electrodynamics, LLC. It received FDA 510(k) clearance on 2017-01-06 under 510(k) number K162946. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the 8ch Knee-Foot SPEEDER?
8ch Knee-Foot SPEEDER is a medical device that received FDA 510(k) clearance on 2017-01-06. The listed applicant is Quality Electrodynamics, LLC. The 510(k) number is K162946.
When did 8ch Knee-Foot SPEEDER receive FDA 510(k) clearance?
8ch Knee-Foot SPEEDER received FDA 510(k) clearance on 2017-01-06, under 510(k) number K162946.
Who is the listed applicant for 8ch Knee-Foot SPEEDER?
The FDA 510(k) record lists Quality Electrodynamics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 8ch Knee-Foot SPEEDER?
The FDA product code for 8ch Knee-Foot SPEEDER is MOS.
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。
列明Quality Electrodynamics, LLC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：MOS）
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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