VITROS® 自动化解决方案
K号: K160495 · 2016-10-18
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决定日期2016-10-18
产品代码KLI
咨询委员会CH
请注意，您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
VITROS® Automation Solutions is the device name listed in this FDA 510(k) record. The listed applicant is Ortho-Clinical Diagnostics, Inc.. It received FDA 510(k) clearance on 2016-10-18 under 510(k) number K160495. The device is classified under product code KLI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VITROS® Automation Solutions?
VITROS® Automation Solutions is a medical device that received FDA 510(k) clearance on 2016-10-18. The listed applicant is Ortho-Clinical Diagnostics, Inc.. The 510(k) number is K160495.
When did VITROS® Automation Solutions receive FDA 510(k) clearance?
VITROS® Automation Solutions received FDA 510(k) clearance on 2016-10-18, under 510(k) number K160495.
Who is the listed applicant for VITROS® Automation Solutions?
The FDA 510(k) record lists Ortho-Clinical Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITROS® Automation Solutions?
The FDA product code for VITROS® Automation Solutions is KLI.
相关临床试验
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列明Ortho-Clinical Diagnostics, 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。
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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