FDA 510(k)

Actreen Mini 间歇性导尿管

K号: K151772 · 2016-02-09

决定日期2016-02-09

产品代码GBM

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决定实质等同

器械摘要

Actreen Mini Intermittent Urinary Catheters is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2016-02-09 under 510(k) number K151772. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Actreen Mini Intermittent Urinary Catheters?

Actreen Mini Intermittent Urinary Catheters is a medical device that received FDA 510(k) clearance on 2016-02-09. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K151772.

When did Actreen Mini Intermittent Urinary Catheters receive FDA 510(k) clearance?

Actreen Mini Intermittent Urinary Catheters received FDA 510(k) clearance on 2016-02-09, under 510(k) number K151772.

Who is the listed applicant for Actreen Mini Intermittent Urinary Catheters?

FDA 510(k)记录中列出了B.Braun Medical, Inc.为申请人。这本身并不足以确立该设备的制造商。

What is the FDA product code for Actreen Mini Intermittent Urinary Catheters?

The FDA product code for Actreen Mini Intermittent Urinary Catheters is GBM.

列明B.Braun Medical, Inc.为申报人的其他记录

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