FDA 510(k)

Compass可调针

K号: K221206 · 2022-08-25

决定日期2022-08-25

产品代码KTI

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决定实质等同

器械摘要

Compass Steerable Needle is the device name listed in this FDA 510(k) record. The listed applicant is Serpex Medical, Inc.. It received FDA 510(k) clearance on 2022-08-25 under 510(k) number K221206. The device is classified under product code KTI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Compass Steerable Needle?

Compass Steerable Needle is a medical device that received FDA 510(k) clearance on 2022-08-25. The listed applicant is Serpex Medical, Inc.. The 510(k) number is K221206.

When did Compass Steerable Needle receive FDA 510(k) clearance?

Compass Steerable Needle received FDA 510(k) clearance on 2022-08-25, under 510(k) number K221206.

Who is the listed applicant for Compass Steerable Needle?

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

What is the FDA product code for Compass Steerable Needle?

The FDA product code for Compass Steerable Needle is KTI.

列明Serpex Medical, 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。

K252874Compass可调针，配备适配器SRA-1-01和SRA-2-01 K221302Recon Steerable Sheath

相关器械（代码：KTI）

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。

K261274EchoTip Ultra® 内镜超声活检针，适用于富士胶片内窥镜；EchoTip ProCore® 内镜超声活检针，适用于富士胶片内窥镜Cook Ireland, Ltd.K251478ClearTip TBNA 类型Finemedix Co., Ltd.K254040LungFlow篮状导管Free Flow Medical, Inc.K251402LIA-1 Catheter (542-1)Leadoptik, Inc.K252874Compass可调针，配备适配器SRA-1-01和SRA-2-01Serpex Medical, Inc.K251664一次性吸引针（NA-201SX-4021）；一次性吸引针（NA-201SX-4022）Olympus Medical Systems Corporation

官方来源

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