8通道T/R膝关节线圈
K号: K223225 · 2023-02-14
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器械摘要
8ch T/R Knee Coil is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-02-14 under 510(k) number K223225. 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 T/R Knee Coil?
8ch T/R Knee Coil is a medical device that received FDA 510(k) clearance on 2023-02-14. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223225.
When did 8ch T/R Knee Coil receive FDA 510(k) clearance?
8ch T/R Knee Coil received FDA 510(k) clearance on 2023-02-14, under 510(k) number K223225.
Who is the listed applicant for 8ch T/R Knee Coil?
The FDA 510(k) record lists Shenzhen RF Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 8ch T/R Knee Coil?
The FDA product code for 8ch T/R Knee Coil is MOS.
列明Shenzhen RF Tech Co., Ltd.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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