FDA 510(k)

Aesculap Slim Clip Applier

K号: K211572 · 2021-12-13

决定日期2021-12-13

产品代码HCI

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决定实质等同

器械摘要

Aesculap Slim Clip Applier is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2021-12-13 under 510(k) number K211572. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Aesculap Slim Clip Applier?

Aesculap Slim Clip Applier is a medical device that received FDA 510(k) clearance on 2021-12-13. The listed applicant is Aesculap, Inc.. The 510(k) number is K211572.

When did Aesculap Slim Clip Applier receive FDA 510(k) clearance?

Aesculap Slim Clip Applier received FDA 510(k) clearance on 2021-12-13, under 510(k) number K211572.

Who is the listed applicant for Aesculap Slim Clip Applier?

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 Slim Clip Applier?

The FDA product code for Aesculap Slim Clip Applier is HCI.

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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