AXIS 图像管理系统
K号: K171098 · 2017-05-02
广告
器械摘要
AXIS Image Management System is the device name listed in this FDA 510(k) record. The listed applicant is Sonomed, Inc.. It received FDA 510(k) clearance on 2017-05-02 under 510(k) number K171098. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AXIS Image Management System?
AXIS Image Management System is a medical device that received FDA 510(k) clearance on 2017-05-02. The listed applicant is Sonomed, Inc.. The 510(k) number is K171098.
When did AXIS Image Management System receive FDA 510(k) clearance?
AXIS Image Management System received FDA 510(k) clearance on 2017-05-02, under 510(k) number K171098.
Who is the listed applicant for AXIS Image Management System?
The FDA 510(k) record lists Sonomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXIS Image Management System?
The FDA product code for AXIS Image Management System is NFJ.
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。
相关器械（代码：NFJ）
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。
广告