血液透析导管
K号: K241581 · 2025-05-16
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决定日期2025-05-16
产品代码MSD
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定Unknown
器械摘要
Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Haolang Medical USA Corporation. It received FDA 510(k) clearance on 2025-05-16 under 510(k) number K241581. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常见问题
What is the Hemodialysis Catheter?
Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2025-05-16. The listed applicant is Haolang Medical USA Corporation. The 510(k) number is K241581.
When did Hemodialysis Catheter receive FDA 510(k) clearance?
Hemodialysis Catheter received FDA 510(k) clearance on 2025-05-16, under 510(k) number K241581.
Who is the listed applicant for Hemodialysis Catheter?
The FDA 510(k) record lists Haolang Medical USA Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hemodialysis Catheter?
The FDA product code for Hemodialysis Catheter is MSD.
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Haolang Medical USA Corporation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：MSD）
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。
K210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro 长期血液透析导管C.R. Bard, Inc.K211410GlidePath 13F 长期血液透析导管Bard Peripheral Vascular, Inc.K203767Pristine 长期血液透析导管C B Bard, Inc.K202150GlidePath 7.5F 长期透析导管C.R. Bard, Inc.K202176Symetrex LTHD 导管，Symetrex LTHD 导管带侧孔Medical Components, Inc. (dba MedComp)
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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