FDA 510(k)

Sutter Swyng防粘双极镊子，一次性使用

K号: K193587 · 2020-02-10

决定日期2020-02-10

产品代码GEI

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决定实质等同

器械摘要

Sutter Swyng non-stick bipolar forceps, single-use is the device name listed in this FDA 510(k) record. The listed applicant is Sutter Medizintechnik GmbH. It received FDA 510(k) clearance on 2020-02-10 under 510(k) number K193587. 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 Sutter Swyng non-stick bipolar forceps, single-use?

Sutter Swyng non-stick bipolar forceps, single-use is a medical device that received FDA 510(k) clearance on 2020-02-10. The listed applicant is Sutter Medizintechnik GmbH. The 510(k) number is K193587.

When did Sutter Swyng non-stick bipolar forceps, single-use receive FDA 510(k) clearance?

Sutter Swyng non-stick bipolar forceps, single-use received FDA 510(k) clearance on 2020-02-10, under 510(k) number K193587.

Who is the listed applicant for Sutter Swyng non-stick bipolar forceps, single-use?

The FDA 510(k) record lists Sutter Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sutter Swyng non-stick bipolar forceps, single-use?

The FDA product code for Sutter Swyng non-stick bipolar forceps, single-use is GEI.

列明Sutter Medizintechnik GmbH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：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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