SR-2300 便携式 DR 成像系统,SR-2300S 便携式 DR 成像系统
K号: K202353 · 2020-12-23
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器械摘要
常见问题
What is the SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System?
SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System is a medical device that received FDA 510(k) clearance on 2020-12-23. The listed applicant is Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui). The 510(k) number is K202353.
When did SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System receive FDA 510(k) clearance?
SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System received FDA 510(k) clearance on 2020-12-23, under 510(k) number K202353.
Who is the listed applicant for SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System?
The FDA 510(k) record lists Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System?
The FDA product code for SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System is IZL.
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Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui)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:IZL)
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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