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FDA 510(k)

泰坦3低速角度附件

K号: K162397 · 2017-01-19

决定日期2017-01-19
产品代码EGS
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决定实质等同

器械摘要

Titan 3 Low Speed Angle Attachments is the device name listed in this FDA 510(k) record. The listed applicant is Dentalez, Inc.. It received FDA 510(k) clearance on 2017-01-19 under 510(k) number K162397. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Titan 3 Low Speed Angle Attachments?

Titan 3 Low Speed Angle Attachments is a medical device that received FDA 510(k) clearance on 2017-01-19. The listed applicant is Dentalez, Inc.. The 510(k) number is K162397.

When did Titan 3 Low Speed Angle Attachments receive FDA 510(k) clearance?

Titan 3 Low Speed Angle Attachments received FDA 510(k) clearance on 2017-01-19, under 510(k) number K162397.

Who is the listed applicant for Titan 3 Low Speed Angle Attachments?

The FDA 510(k) record lists Dentalez, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Titan 3 Low Speed Angle Attachments?

The FDA product code for Titan 3 Low Speed Angle Attachments is EGS.

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Dentalez, Inc.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:EGS)

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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