VITA YZ ST 和 VITA YZ XT
K号: K180703 · 2018-08-01
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决定日期2018-08-01
产品代码EIH
咨询委员会DE
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决定实质等同
器械摘要
VITA YZ ST and VITA YZ XT is the device name listed in this FDA 510(k) record. The listed applicant is Vita Zahnfabrik H.Rauter GmbH Co.. It received FDA 510(k) clearance on 2018-08-01 under 510(k) number K180703. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VITA YZ ST and VITA YZ XT?
VITA YZ ST and VITA YZ XT is a medical device that received FDA 510(k) clearance on 2018-08-01. The listed applicant is Vita Zahnfabrik H.Rauter GmbH Co.. The 510(k) number is K180703.
When did VITA YZ ST and VITA YZ XT receive FDA 510(k) clearance?
VITA YZ ST and VITA YZ XT received FDA 510(k) clearance on 2018-08-01, under 510(k) number K180703.
Who is the listed applicant for VITA YZ ST and VITA YZ XT?
The FDA 510(k) record lists Vita Zahnfabrik H.Rauter GmbH Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITA YZ ST and VITA YZ XT?
The FDA product code for VITA YZ ST and VITA YZ XT is EIH.
列明Vita Zahnfabrik H.Rauter GmbH Co.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：EIH）
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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