ZMAXX 牙科氧化锆片
K号: K191631 · 2019-11-01
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决定日期2019-11-01
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
ZMAXX Dental Zirconia Blanks is the device name listed in this FDA 510(k) record. The listed applicant is Zmaxx Bioceramics, LLC. It received FDA 510(k) clearance on 2019-11-01 under 510(k) number K191631. 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 ZMAXX Dental Zirconia Blanks?
ZMAXX Dental Zirconia Blanks is a medical device that received FDA 510(k) clearance on 2019-11-01. The listed applicant is Zmaxx Bioceramics, LLC. The 510(k) number is K191631.
When did ZMAXX Dental Zirconia Blanks receive FDA 510(k) clearance?
ZMAXX Dental Zirconia Blanks received FDA 510(k) clearance on 2019-11-01, under 510(k) number K191631.
Who is the listed applicant for ZMAXX Dental Zirconia Blanks?
The FDA 510(k) record lists Zmaxx Bioceramics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZMAXX Dental Zirconia Blanks?
The FDA product code for ZMAXX Dental Zirconia Blanks is EIH.
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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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