OEC 3D
K号: K233669 · 2024-03-28
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器械摘要
OEC 3D is the device name listed in this FDA 510(k) record. The listed applicant is Ge Oec Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-03-28 under 510(k) number K233669. 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 3D?
OEC 3D is a medical device that received FDA 510(k) clearance on 2024-03-28. The listed applicant is Ge Oec Medical Systems, Inc.. The 510(k) number is K233669.
When did OEC 3D receive FDA 510(k) clearance?
OEC 3D received FDA 510(k) clearance on 2024-03-28, under 510(k) number K233669.
Who is the listed applicant for OEC 3D?
The FDA 510(k) record lists Ge Oec Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OEC 3D?
The FDA product code for OEC 3D is OXO.
列明Ge Oec Medical Systems, 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：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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