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FDA 510(k)

KLS Martin 口腔-Max 嵌入物 MR 条件性(捆绑)

K号: K241314 · 2024-08-16

决定日期2024-08-16
产品代码JEY
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决定实质等同

器械摘要

KLS Martin Oral-Max Implants MR Conditional (bundled) is the device name listed in this FDA 510(k) record. The listed applicant is KLS-Martin L.P.. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K241314. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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。

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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

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