Vita Flex CR 系统，带 LLI
K号: K192894 · 2020-02-18
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器械摘要
Vita Flex CR System with LLI is the device name listed in this FDA 510(k) record. The listed applicant is Carestream Health, Inc.. It received FDA 510(k) clearance on 2020-02-18 under 510(k) number K192894. 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 Vita Flex CR System with LLI?
Vita Flex CR System with LLI is a medical device that received FDA 510(k) clearance on 2020-02-18. The listed applicant is Carestream Health, Inc.. The 510(k) number is K192894.
When did Vita Flex CR System with LLI receive FDA 510(k) clearance?
Vita Flex CR System with LLI received FDA 510(k) clearance on 2020-02-18, under 510(k) number K192894.
Who is the listed applicant for Vita Flex CR System with LLI?
The FDA 510(k) record lists Carestream Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vita Flex CR System with LLI?
The FDA product code for Vita Flex CR System with LLI is MQB.
相关临床试验
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列明Carestream Health, 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：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。
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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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