Revolution Ascend Sliding
K号: K233749 · 2024-02-22
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器械摘要
Revolution Ascend Sliding is the device name listed in this FDA 510(k) record. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K233749. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Revolution Ascend Sliding?
Revolution Ascend Sliding is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. The 510(k) number is K233749.
When did Revolution Ascend Sliding receive FDA 510(k) clearance?
Revolution Ascend Sliding received FDA 510(k) clearance on 2024-02-22, under 510(k) number K233749.
Who is the listed applicant for Revolution Ascend Sliding?
The FDA 510(k) record lists Ge Hangwei Medical Systems Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Revolution Ascend Sliding?
The FDA product code for Revolution Ascend Sliding is JAK.
相关临床试验
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列明Ge Hangwei Medical Systems 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：JAK）
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
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