Infinix-i, INFX-8000V, V7.0
K号: K172863 · 2017-12-14
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器械摘要
Infinix-i, INFX-8000V, V7.0 is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-12-14 under 510(k) number K172863. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Infinix-i, INFX-8000V, V7.0?
Infinix-i, INFX-8000V, V7.0 is a medical device that received FDA 510(k) clearance on 2017-12-14. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K172863.
When did Infinix-i, INFX-8000V, V7.0 receive FDA 510(k) clearance?
Infinix-i, INFX-8000V, V7.0 received FDA 510(k) clearance on 2017-12-14, under 510(k) number K172863.
Who is the listed applicant for Infinix-i, INFX-8000V, V7.0?
The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Infinix-i, INFX-8000V, V7.0?
The FDA product code for Infinix-i, INFX-8000V, V7.0 is OWB.
相关临床试验
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列明Toshibamedical Systems Corporation为申报人的其他记录
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相关器械（代码：OWB）
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。
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