FDA 510(k)

GlidePath Retro 长期血液透析导管

K号: K203575 · 2021-07-01

决定日期2021-07-01

产品代码MSD

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决定Unknown

器械摘要

GlidePath Retro Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2021-07-01 under 510(k) number K203575. 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 GlidePath Retro Long-Term Hemodialysis Catheter?

GlidePath Retro Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-07-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K203575.

When did GlidePath Retro Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?

GlidePath Retro Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-07-01, under 510(k) number K203575.

Who is the listed applicant for GlidePath Retro Long-Term Hemodialysis Catheter?

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

What is the FDA product code for GlidePath Retro Long-Term Hemodialysis Catheter?

The FDA product code for GlidePath Retro Long-Term Hemodialysis Catheter is MSD.

列明C.R. Bard, 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。

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