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)

带ENFit连接器的口腔/肠内注射器

K号: K222772 · 2023-08-17

决定日期2023-08-17
产品代码PNR
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

Oral/Enteral Syringe with ENFit connector is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-08-17 under 510(k) number K222772. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Oral/Enteral Syringe with ENFit connector?

Oral/Enteral Syringe with ENFit connector is a medical device that received FDA 510(k) clearance on 2023-08-17. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K222772.

When did Oral/Enteral Syringe with ENFit connector receive FDA 510(k) clearance?

Oral/Enteral Syringe with ENFit connector received FDA 510(k) clearance on 2023-08-17, under 510(k) number K222772.

Who is the listed applicant for Oral/Enteral Syringe with ENFit connector?

The FDA 510(k) record lists Anhui Tiankang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oral/Enteral Syringe with ENFit connector?

The FDA product code for Oral/Enteral Syringe with ENFit connector is PNR.

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Anhui Tiankang Medical Technology 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。

查看所有 12 个设备 →

相关器械(代码:PNR)

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。

↑