16通道发射/接收膝关节SPEEDER
K号: K161193 · 2016-06-02
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器械摘要
16ch Tx/Rx Knee 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 2016-06-02 under 510(k) number K161193. 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 16ch Tx/Rx Knee SPEEDER?
16ch Tx/Rx Knee SPEEDER is a medical device that received FDA 510(k) clearance on 2016-06-02. The listed applicant is Quality Electrodynamics, LLC. The 510(k) number is K161193.
When did 16ch Tx/Rx Knee SPEEDER receive FDA 510(k) clearance?
16ch Tx/Rx Knee SPEEDER received FDA 510(k) clearance on 2016-06-02, under 510(k) number K161193.
Who is the listed applicant for 16ch Tx/Rx Knee 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 16ch Tx/Rx Knee SPEEDER?
The FDA product code for 16ch Tx/Rx Knee 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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