Ivotion Base Print
K号: K233995 · 2024-02-23
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决定日期2024-02-23
产品代码EBI
咨询委员会DE
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器械摘要
Ivotion Base Print is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2024-02-23 under 510(k) number K233995. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Ivotion Base Print?
Ivotion Base Print is a medical device that received FDA 510(k) clearance on 2024-02-23. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K233995.
When did Ivotion Base Print receive FDA 510(k) clearance?
Ivotion Base Print received FDA 510(k) clearance on 2024-02-23, under 510(k) number K233995.
Who is the listed applicant for Ivotion Base Print?
The FDA 510(k) record lists Ivoclar Vivadent, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ivotion Base Print?
The FDA product code for Ivotion Base Print is EBI.
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Ivoclar Vivadent, 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：EBI）
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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