HF1202H PowerPlus 便携式X射线设备
K号: K153059 · 2016-02-02
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器械摘要
HF1202H PowerPlus Portable X-ray Equipment is the device name listed in this FDA 510(k) record. The listed applicant is Minxray, Inc.. It received FDA 510(k) clearance on 2016-02-02 under 510(k) number K153059. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the HF1202H PowerPlus Portable X-ray Equipment?
HF1202H PowerPlus Portable X-ray Equipment is a medical device that received FDA 510(k) clearance on 2016-02-02. The listed applicant is Minxray, Inc.. The 510(k) number is K153059.
When did HF1202H PowerPlus Portable X-ray Equipment receive FDA 510(k) clearance?
HF1202H PowerPlus Portable X-ray Equipment received FDA 510(k) clearance on 2016-02-02, under 510(k) number K153059.
Who is the listed applicant for HF1202H PowerPlus Portable X-ray Equipment?
The FDA 510(k) record lists Minxray, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HF1202H PowerPlus Portable X-ray Equipment?
The FDA product code for HF1202H PowerPlus Portable X-ray Equipment 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Minxray, 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：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。
K260236XLITEGEMSS HEALTHCARE CO., LTD.K253058便携式DR成像系统Shantou Institute of Ultrasonic Instruments Co., Ltd.K260085RAYMO 移动X光系统（型号：RAYMO）DRGEM CorporationK253185Lux HD 探测器，DRX-LC 探测器，DRX-Revolution 移动X射线系统Carestream HealthK253244AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F（AirRay-mini）Poskom Co., Ltd.K250976Airbile-100Poskom Co., Ltd.
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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