CS 9600
K号: K200183 · 2020-03-13
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器械摘要
CS 9600 is the device name listed in this FDA 510(k) record. The listed applicant is Trophy. It received FDA 510(k) clearance on 2020-03-13 under 510(k) number K200183. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CS 9600?
CS 9600 is a medical device that received FDA 510(k) clearance on 2020-03-13. The listed applicant is Trophy. The 510(k) number is K200183.
When did CS 9600 receive FDA 510(k) clearance?
CS 9600 received FDA 510(k) clearance on 2020-03-13, under 510(k) number K200183.
Who is the listed applicant for CS 9600?
The FDA 510(k) record lists Trophy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CS 9600?
The FDA product code for CS 9600 is OAS.
列明Trophy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：OAS）
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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