VIVIX-S 1717V
K号: K181003 · 2018-05-15
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器械摘要
VIVIX-S 1717V is the device name listed in this FDA 510(k) record. The listed applicant is Vieworks Co., Ltd.. It received FDA 510(k) clearance on 2018-05-15 under 510(k) number K181003. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VIVIX-S 1717V?
VIVIX-S 1717V is a medical device that received FDA 510(k) clearance on 2018-05-15. The listed applicant is Vieworks Co., Ltd.. The 510(k) number is K181003.
When did VIVIX-S 1717V receive FDA 510(k) clearance?
VIVIX-S 1717V received FDA 510(k) clearance on 2018-05-15, under 510(k) number K181003.
Who is the listed applicant for VIVIX-S 1717V?
The FDA 510(k) record lists Vieworks Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIVIX-S 1717V?
The FDA product code for VIVIX-S 1717V is MQB.
相关临床试验
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列明Vieworks 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：MQB）
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。
K2538000909FCE，0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996通用 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 探测器 (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211玉山X射线平板探测器Innocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, 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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