C.C. LIFE 21
K号: K213295 · 2022-11-17
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决定日期2022-11-17
产品代码PBX
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
C.C. LIFE 21 is the device name listed in this FDA 510(k) record. The listed applicant is 21 Equipment S.R.L.. It received FDA 510(k) clearance on 2022-11-17 under 510(k) number K213295. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the C.C. LIFE 21?
C.C. LIFE 21 is a medical device that received FDA 510(k) clearance on 2022-11-17. The listed applicant is 21 Equipment S.R.L.. The 510(k) number is K213295.
When did C.C. LIFE 21 receive FDA 510(k) clearance?
C.C. LIFE 21 received FDA 510(k) clearance on 2022-11-17, under 510(k) number K213295.
Who is the listed applicant for C.C. LIFE 21?
The FDA 510(k) record lists 21 Equipment S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C.C. LIFE 21?
The FDA product code for C.C. LIFE 21 is PBX.
列明21 Equipment S.R.L.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：PBX）
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。
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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