免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Cedic 肠内 ENFit 过渡连接器

K号: K162254 · 2017-05-04

申请人Cedic S.R.L.
决定日期2017-05-04
产品代码PIO
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。
决定实质等同

器械摘要

Cedic Enteral ENFit Transition Connectors is the device name listed in this FDA 510(k) record. The listed applicant is Cedic S.R.L.. It received FDA 510(k) clearance on 2017-05-04 under 510(k) number K162254. The device is classified under product code PIO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Cedic Enteral ENFit Transition Connectors?

Cedic Enteral ENFit Transition Connectors is a medical device that received FDA 510(k) clearance on 2017-05-04. The listed applicant is Cedic S.R.L.. The 510(k) number is K162254.

When did Cedic Enteral ENFit Transition Connectors receive FDA 510(k) clearance?

Cedic Enteral ENFit Transition Connectors received FDA 510(k) clearance on 2017-05-04, under 510(k) number K162254.

Who is the listed applicant for Cedic Enteral ENFit Transition Connectors?

The FDA 510(k) record lists Cedic S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cedic Enteral ENFit Transition Connectors?

The FDA product code for Cedic Enteral ENFit Transition Connectors is PIO.

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Cedic S.R.L.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:PIO)

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。

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。

↑