Profound Matrix
K号: K211217 · 2021-12-16
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决定日期2021-12-16
产品代码GEI
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Profound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Candela Corporation. It received FDA 510(k) clearance on 2021-12-16 under 510(k) number K211217. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Profound Matrix?
Profound Matrix is a medical device that received FDA 510(k) clearance on 2021-12-16. The listed applicant is Candela Corporation. The 510(k) number is K211217.
When did Profound Matrix receive FDA 510(k) clearance?
Profound Matrix received FDA 510(k) clearance on 2021-12-16, under 510(k) number K211217.
Who is the listed applicant for Profound Matrix?
The FDA 510(k) record lists Candela Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Profound Matrix?
The FDA product code for Profound Matrix is GEI.
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Candela Corporation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：GEI）
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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