FDA 510(k)

双腔卵泡吸取针

K号: K171611 · 2017-12-15

申请人William A. Cook Australia Pty. , Ltd.

决定日期2017-12-15

产品代码MQE

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决定实质等同

器械摘要

Double Lumen Ovum Aspiration Needles is the device name listed in this FDA 510(k) record. The listed applicant is William A. Cook Australia Pty. , Ltd.. It received FDA 510(k) clearance on 2017-12-15 under 510(k) number K171611. The device is classified under product code MQE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Double Lumen Ovum Aspiration Needles?

Double Lumen Ovum Aspiration Needles is a medical device that received FDA 510(k) clearance on 2017-12-15. The listed applicant is William A. Cook Australia Pty. , Ltd.. The 510(k) number is K171611.

When did Double Lumen Ovum Aspiration Needles receive FDA 510(k) clearance?

Double Lumen Ovum Aspiration Needles received FDA 510(k) clearance on 2017-12-15, under 510(k) number K171611.

Who is the listed applicant for Double Lumen Ovum Aspiration Needles?

The FDA 510(k) record lists William A. Cook Australia Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Double Lumen Ovum Aspiration Needles?

The FDA product code for Double Lumen Ovum Aspiration Needles is MQE.

列明William A. Cook Australia Pty. , Ltd.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：MQE）

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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