VITA VIONIC 粘合剂
K号: K191926 · 2020-01-29
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决定日期2020-01-29
产品代码EBI
咨询委员会DE
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决定实质等同
器械摘要
VITA VIONIC Bond is the device name listed in this FDA 510(k) record. The listed applicant is Vita Zanhnfabrik H. Rauter GmbH Co.. It received FDA 510(k) clearance on 2020-01-29 under 510(k) number K191926. 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 VITA VIONIC Bond?
VITA VIONIC Bond is a medical device that received FDA 510(k) clearance on 2020-01-29. The listed applicant is Vita Zanhnfabrik H. Rauter GmbH Co.. The 510(k) number is K191926.
When did VITA VIONIC Bond receive FDA 510(k) clearance?
VITA VIONIC Bond received FDA 510(k) clearance on 2020-01-29, under 510(k) number K191926.
Who is the listed applicant for VITA VIONIC Bond?
The FDA 510(k) record lists Vita Zanhnfabrik H. Rauter GmbH Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITA VIONIC Bond?
The FDA product code for VITA VIONIC Bond 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。
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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