Clarus Peel-Away 引导鞘
K号: K200925 · 2021-03-18
广告
决定日期2021-03-18
产品代码GWG
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Clarus Peel-Away Introducer Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Clarus Medical, LLC. It received FDA 510(k) clearance on 2021-03-18 under 510(k) number K200925. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Clarus Peel-Away Introducer Sheath?
Clarus Peel-Away Introducer Sheath is a medical device that received FDA 510(k) clearance on 2021-03-18. The listed applicant is Clarus Medical, LLC. The 510(k) number is K200925.
When did Clarus Peel-Away Introducer Sheath receive FDA 510(k) clearance?
Clarus Peel-Away Introducer Sheath received FDA 510(k) clearance on 2021-03-18, under 510(k) number K200925.
Who is the listed applicant for Clarus Peel-Away Introducer Sheath?
The FDA 510(k) record lists Clarus Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clarus Peel-Away Introducer Sheath?
The FDA product code for Clarus Peel-Away Introducer Sheath is GWG.
相关临床试验
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。
列明Clarus Medical, LLC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。
相关器械（代码：GWG）
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。
K253602Precision S 4K SinuscopeStryker EndoscopyK253679Hydro 灌洗系统Stryker InstrumentsK243429HJY VisualNext 3D 内窥镜视觉系统Hjy Smart Medical Device Co., Ltd.K250752AURORA® Surgiscope® 系统（ASX15/60）；AURORA® Surgiscope® 系统（ASX15/80）Integra LifeSciences CorporationK233391cCeLL - 在体VPIX Medical, Inc.K223615数字ClarusScope系统，数字NeuroPEN系统Clarus Medical, LLC
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
广告