托克体
K号: K192039 · 2020-03-29
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决定日期2020-03-29
产品代码NGX
咨询委员会PM
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决定实质等同
器械摘要
Torc Body is the device name listed in this FDA 510(k) record. The listed applicant is Johari Digital Healthcare Limited. It received FDA 510(k) clearance on 2020-03-29 under 510(k) number K192039. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Torc Body?
Torc Body is a medical device that received FDA 510(k) clearance on 2020-03-29. The listed applicant is Johari Digital Healthcare Limited. The 510(k) number is K192039.
When did Torc Body receive FDA 510(k) clearance?
Torc Body received FDA 510(k) clearance on 2020-03-29, under 510(k) number K192039.
Who is the listed applicant for Torc Body?
The FDA 510(k) record lists Johari Digital Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Torc Body?
The FDA product code for Torc Body is NGX.
列明Johari Digital Healthcare Limited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：NGX）
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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