Versus™ 导管（VS110-9NB）
K号: K260149 · 2026-02-17
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决定日期2026-02-17
产品代码QEY
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
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产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
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请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同
器械摘要
Versus™ Catheter (VS110-9NB) is the device name listed in this FDA 510(k) record. The listed applicant is Liquet Medical, Inc.. It received FDA 510(k) clearance on 2026-02-17 under 510(k) number K260149. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Versus™ Catheter (VS110-9NB)?
Versus™ Catheter (VS110-9NB) is a medical device that received FDA 510(k) clearance on 2026-02-17. The listed applicant is Liquet Medical, Inc.. The 510(k) number is K260149.
When did Versus™ Catheter (VS110-9NB) receive FDA 510(k) clearance?
Versus™ Catheter (VS110-9NB) received FDA 510(k) clearance on 2026-02-17, under 510(k) number K260149.
Who is the listed applicant for Versus™ Catheter (VS110-9NB)?
The FDA 510(k) record lists Liquet Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Versus™ Catheter (VS110-9NB)?
The FDA product code for Versus™ Catheter (VS110-9NB) is QEY.
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Liquet Medical, 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。
相关器械（代码：QEY）
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。
K251318VariFuse 可调式输液导管Argon Medical Devices, Inc.K241851Versus™ 导管（VS110-8B）Liquet Medical, Inc.K231653BASHIR™ .035 内窥镜导管，BASHIR™ S-B .035 内窥镜导管Thrombolex, Inc.K222095BASHIR 内窥镜导管参考编号 7201，BASHIR S-B 内窥镜导管，参考编号 7101Thrombolex, Inc.K220866EKOS+ 内血管设备Boston ScientificK213422EkoSonic Endovascular Device, EKOS+ Endovascular DeviceBoston Scientific Corporation
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。
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