FDA 510(k)

一次性单极腹腔镜轴和可重复使用手柄

K号: K210569 · 2021-08-16

决定日期2021-08-16

产品代码GEI

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决定实质等同

器械摘要

Disposable Monopolar Laparoscopic Shafts and Reusable Handles is the device name listed in this FDA 510(k) record. The listed applicant is Dannik, LLC. It received FDA 510(k) clearance on 2021-08-16 under 510(k) number K210569. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Disposable Monopolar Laparoscopic Shafts and Reusable Handles?

Disposable Monopolar Laparoscopic Shafts and Reusable Handles is a medical device that received FDA 510(k) clearance on 2021-08-16. The listed applicant is Dannik, LLC. The 510(k) number is K210569.

When did Disposable Monopolar Laparoscopic Shafts and Reusable Handles receive FDA 510(k) clearance?

Disposable Monopolar Laparoscopic Shafts and Reusable Handles received FDA 510(k) clearance on 2021-08-16, under 510(k) number K210569.

Who is the listed applicant for Disposable Monopolar Laparoscopic Shafts and Reusable Handles?

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

What is the FDA product code for Disposable Monopolar Laparoscopic Shafts and Reusable Handles?

The FDA product code for Disposable Monopolar Laparoscopic Shafts and Reusable Handles is GEI.

列明Dannik, 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。

K250411DANNIK® 腹腔镜单次使用多聚标本采集系统 K211019一次性单极腹腔镜尖端和可重复使用手柄

相关器械（代码：GEI）

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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