Veraview X800
K号: K171012 · 2017-12-19
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器械摘要
Veraview X800 is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K171012. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Veraview X800?
Veraview X800 is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K171012.
When did Veraview X800 receive FDA 510(k) clearance?
Veraview X800 received FDA 510(k) clearance on 2017-12-19, under 510(k) number K171012.
Who is the listed applicant for Veraview X800?
The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Veraview X800?
The FDA product code for Veraview X800 is OAS.
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J. Morita USA, 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：OAS）
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。
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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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