Cios Spin
K号: K210054 · 2021-02-05
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器械摘要
Cios Spin is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Systems USA, Inc.. It received FDA 510(k) clearance on 2021-02-05 under 510(k) number K210054. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cios Spin?
Cios Spin is a medical device that received FDA 510(k) clearance on 2021-02-05. The listed applicant is Siemens Medical Systems USA, Inc.. The 510(k) number is K210054.
When did Cios Spin receive FDA 510(k) clearance?
Cios Spin received FDA 510(k) clearance on 2021-02-05, under 510(k) number K210054.
Who is the listed applicant for Cios Spin?
The FDA 510(k) record lists Siemens Medical Systems USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cios Spin?
The FDA product code for Cios Spin is OWB.
列明Siemens Medical Systems USA, Inc.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：OWB）
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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