FDA 510(k)

SQ.line KERRISON

K号: K223596 · 2023-06-29

决定日期2023-06-29

产品代码HAE

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决定实质等同

器械摘要

SQ.line KERRISON is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2023-06-29 under 510(k) number K223596. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SQ.line KERRISON?

SQ.line KERRISON is a medical device that received FDA 510(k) clearance on 2023-06-29. The listed applicant is Aesculap, Inc.. The 510(k) number is K223596.

When did SQ.line KERRISON receive FDA 510(k) clearance?

SQ.line KERRISON received FDA 510(k) clearance on 2023-06-29, under 510(k) number K223596.

Who is the listed applicant for SQ.line KERRISON?

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 SQ.line KERRISON?

The FDA product code for SQ.line KERRISON is HAE.

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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