FDA 510(k)

紧凑Cath间歇性导尿管

K号: K160858 · 2016-04-26

决定日期2016-04-26

产品代码EZD

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决定实质等同

器械摘要

CompactCath Intermittent Urinary Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Compactcath, Inc.. It received FDA 510(k) clearance on 2016-04-26 under 510(k) number K160858. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CompactCath Intermittent Urinary Catheter?

CompactCath Intermittent Urinary Catheter is a medical device that received FDA 510(k) clearance on 2016-04-26. The listed applicant is Compactcath, Inc.. The 510(k) number is K160858.

When did CompactCath Intermittent Urinary Catheter receive FDA 510(k) clearance?

CompactCath Intermittent Urinary Catheter received FDA 510(k) clearance on 2016-04-26, under 510(k) number K160858.

Who is the listed applicant for CompactCath Intermittent Urinary Catheter?

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

What is the FDA product code for CompactCath Intermittent Urinary Catheter?

The FDA product code for CompactCath Intermittent Urinary Catheter is EZD.

列明Compactcath, 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。

K180738COMPACTCATH 润滑间歇导尿管和 OneCath 间歇导尿管

相关器械（代码：EZD）

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。

K261418Liquick X-treme，Liquick X-treme PlusTeleflex Medical K260737Cure Aqua™ 即用型亲水性间歇导尿管女性用（CH06 - CH16）；Cure Aqua™ 即用型亲水性间歇导尿管男性直型（CH06 - CH18）；Cure Aqua™ 即用型亲水性间歇导尿管男性弯型（CH10 - CH18）。Convatec K261658LoFric Origo Pro CoudéWellspect AB K262045Luja软性产品Coloplast A.S.K260394一次性使用亲水性涂层间歇性纳拉通导尿管（NCR）Hangzhou Jimushi Meditech Co., Ltd.K253295Coude袖套IC；Coude Plus袖套ICHollister Incorporated

官方来源

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