FDA 510(k)

Aesculap Caiman 12 密封和切割技术系统

K号: K203461 · 2020-12-18

决定日期2020-12-18

产品代码GEI

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决定实质等同

器械摘要

Aesculap Caiman 12 Seal and Cut Technology System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-12-18 under 510(k) number K203461. 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 Aesculap Caiman 12 Seal and Cut Technology System?

Aesculap Caiman 12 Seal and Cut Technology System is a medical device that received FDA 510(k) clearance on 2020-12-18. The listed applicant is Aesculap, Inc.. The 510(k) number is K203461.

When did Aesculap Caiman 12 Seal and Cut Technology System receive FDA 510(k) clearance?

Aesculap Caiman 12 Seal and Cut Technology System received FDA 510(k) clearance on 2020-12-18, under 510(k) number K203461.

Who is the listed applicant for Aesculap Caiman 12 Seal and Cut Technology System?

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

What is the FDA product code for Aesculap Caiman 12 Seal and Cut Technology System?

The FDA product code for Aesculap Caiman 12 Seal and Cut Technology System is GEI.

列明Aesculap, 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。

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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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