KeyPrint KeyDenture Base
K号: K241089 · 2024-10-24
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决定日期2024-10-24
产品代码EBI
咨询委员会DE
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器械摘要
KeyPrint KeyDenture Base is the device name listed in this FDA 510(k) record. The listed applicant is Keystone Industries. It received FDA 510(k) clearance on 2024-10-24 under 510(k) number K241089. 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 KeyPrint KeyDenture Base?
KeyPrint KeyDenture Base is a medical device that received FDA 510(k) clearance on 2024-10-24. The listed applicant is Keystone Industries. The 510(k) number is K241089.
When did KeyPrint KeyDenture Base receive FDA 510(k) clearance?
KeyPrint KeyDenture Base received FDA 510(k) clearance on 2024-10-24, under 510(k) number K241089.
Who is the listed applicant for KeyPrint KeyDenture Base?
The FDA 510(k) record lists Keystone Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KeyPrint KeyDenture Base?
The FDA product code for KeyPrint KeyDenture Base is EBI.
相关临床试验
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列明Keystone Industries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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