PRIMO S
K号: K211542 · 2021-07-09
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器械摘要
PRIMO S is the device name listed in this FDA 510(k) record. The listed applicant is A.T.S. Applicazione Tecnologie Speciali S.R.L.. It received FDA 510(k) clearance on 2021-07-09 under 510(k) number K211542. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PRIMO S?
PRIMO S is a medical device that received FDA 510(k) clearance on 2021-07-09. The listed applicant is A.T.S. Applicazione Tecnologie Speciali S.R.L.. The 510(k) number is K211542.
When did PRIMO S receive FDA 510(k) clearance?
PRIMO S received FDA 510(k) clearance on 2021-07-09, under 510(k) number K211542.
Who is the listed applicant for PRIMO S?
The FDA 510(k) record lists A.T.S. Applicazione Tecnologie Speciali S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMO S?
The FDA product code for PRIMO S is MQB.
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A.T.S. Applicazione Tecnologie Speciali 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：MQB）
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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