Pristine 长期血液透析导管
K号: K203767 · 2021-04-02
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决定日期2021-04-02
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
Pristine Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C B Bard, Inc.. It received FDA 510(k) clearance on 2021-04-02 under 510(k) number K203767. 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 Pristine Long-Term Hemodialysis Catheter?
Pristine Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is C B Bard, Inc.. The 510(k) number is K203767.
When did Pristine Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?
Pristine Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-04-02, under 510(k) number K203767.
Who is the listed applicant for Pristine Long-Term Hemodialysis Catheter?
The FDA 510(k) record lists C B Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pristine Long-Term Hemodialysis Catheter?
The FDA product code for Pristine Long-Term 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。
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。
K241581血液透析导管Haolang Medical USA CorporationK210461End 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.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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