OEC Elite MiniView
K号: K160131 · 2016-06-21
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器械摘要
OEC Elite MiniView is the device name listed in this FDA 510(k) record. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. It received FDA 510(k) clearance on 2016-06-21 under 510(k) number K160131. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the OEC Elite MiniView?
OEC Elite MiniView is a medical device that received FDA 510(k) clearance on 2016-06-21. The listed applicant is Ge Hangwei Medical Systems Co., Ltd.. The 510(k) number is K160131.
When did OEC Elite MiniView receive FDA 510(k) clearance?
OEC Elite MiniView received FDA 510(k) clearance on 2016-06-21, under 510(k) number K160131.
Who is the listed applicant for OEC Elite MiniView?
The FDA 510(k) record lists Ge Hangwei Medical Systems Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OEC Elite MiniView?
The FDA product code for OEC Elite MiniView is OXO.
相关临床试验
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列明Ge Hangwei Medical Systems Co., Ltd.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：OXO）
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。
K2532963D数字C-ARMAllengers Medical Systems LimitedK252579Orthoscan TAU MVP Mini C-Arm SystemZiehm-Orthoscan, Inc.K253269OEC One CFDGe Hualun Medical Systems Co. , Ltd.K251004双模式移动C-臂（Geelin500A，Geelin500M）Hefei Chimed Intelligent Machine Co., Ltd.K250587Orthoscan TAU Mini C-ArmZiehm-Orthoscan, Inc.K243452Orthoscan VERSA Mini C-ArmZiehm-Orthoscan, Inc.
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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