FDA 510(k)

肠内营养导管

K号: K202748 · 2021-04-09

决定日期2021-04-09

产品代码KNT

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决定实质等同

器械摘要

Enteral Feeding Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medcaptain Life Science Co., Ltd.. It received FDA 510(k) clearance on 2021-04-09 under 510(k) number K202748. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Enteral Feeding Catheter?

Enteral Feeding Catheter is a medical device that received FDA 510(k) clearance on 2021-04-09. The listed applicant is Medcaptain Life Science Co., Ltd.. The 510(k) number is K202748.

When did Enteral Feeding Catheter receive FDA 510(k) clearance?

Enteral Feeding Catheter received FDA 510(k) clearance on 2021-04-09, under 510(k) number K202748.

Who is the listed applicant for Enteral Feeding Catheter?

The FDA 510(k) record lists Medcaptain Life Science Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Enteral Feeding Catheter?

The FDA product code for Enteral Feeding Catheter is KNT.

列明Medcaptain Life Science Co., Ltd.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。

K230528扩展套装 K213004无针连接器 K202578KardiFlex NC冠状动脉扩张导管 K202619KardiFlex PTCA球囊扩张导管

相关器械（代码：KNT）

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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