FDA 510(k)

Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula

K号: K170660 · 2017-07-13

决定日期2017-07-13

产品代码HIH

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决定实质等同

器械摘要

Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2017-07-13 under 510(k) number K170660. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula?

Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula is a medical device that received FDA 510(k) clearance on 2017-07-13. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K170660.

When did Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula receive FDA 510(k) clearance?

Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula received FDA 510(k) clearance on 2017-07-13, under 510(k) number K170660.

Who is the listed applicant for Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula?

FDA 510(k)记录中列出CooperSurgical, Inc.为申请人。这本身并不足以确立设备制造商。

What is the FDA product code for Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula?

The FDA product code for Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula is HIH.

列明CooperSurgical, 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：HIH）

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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