Clear Guide SCENERGY
K号: K234030 · 2024-01-17
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器械摘要
Clear Guide SCENERGY is the device name listed in this FDA 510(k) record. The listed applicant is Clear Guide Medical. It received FDA 510(k) clearance on 2024-01-17 under 510(k) number K234030. 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 Clear Guide SCENERGY?
Clear Guide SCENERGY is a medical device that received FDA 510(k) clearance on 2024-01-17. The listed applicant is Clear Guide Medical. The 510(k) number is K234030.
When did Clear Guide SCENERGY receive FDA 510(k) clearance?
Clear Guide SCENERGY received FDA 510(k) clearance on 2024-01-17, under 510(k) number K234030.
Who is the listed applicant for Clear Guide SCENERGY?
The FDA 510(k) record lists Clear Guide Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clear Guide SCENERGY?
The FDA product code for Clear Guide SCENERGY is JAK.
相关临床试验
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列明Clear Guide Medical为申报人的其他记录
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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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