KLS Martin 口腔-Max 嵌入物 MR 条件性(捆绑)
K号: K241314 · 2024-08-16
广告
器械摘要
常见问题
What is the KLS Martin Oral-Max Implants MR Conditional (bundled)?
KLS Martin Oral-Max Implants MR Conditional (bundled) is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is KLS-Martin L.P.. The 510(k) number is K241314.
When did KLS Martin Oral-Max Implants MR Conditional (bundled) receive FDA 510(k) clearance?
KLS Martin Oral-Max Implants MR Conditional (bundled) received FDA 510(k) clearance on 2024-08-16, under 510(k) number K241314.
Who is the listed applicant for KLS Martin Oral-Max Implants MR Conditional (bundled)?
FDA 510(k)记录中列出KLS-Martin L.P.为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for KLS Martin Oral-Max Implants MR Conditional (bundled)?
The FDA product code for KLS Martin Oral-Max Implants MR Conditional (bundled) is JEY.
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KLS-Martin L.P.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:JEY)
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。
广告