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FDA 510(k)

3.3毫米Laurimed微切除器;4.0毫米Laurimed微切除器

K号: K163247 · 2017-03-09

申请人Laurimed, LLC
决定日期2017-03-09
产品代码ERL
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决定实质等同

器械摘要

3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider is the device name listed in this FDA 510(k) record. The listed applicant is Laurimed, LLC. It received FDA 510(k) clearance on 2017-03-09 under 510(k) number K163247. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider?

3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Laurimed, LLC. The 510(k) number is K163247.

When did 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider receive FDA 510(k) clearance?

3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider received FDA 510(k) clearance on 2017-03-09, under 510(k) number K163247.

Who is the listed applicant for 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider?

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

What is the FDA product code for 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider?

The FDA product code for 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider is ERL.

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Laurimed, LLC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:ERL)

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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