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FDA 510(k)

无菌一次性使用LDV注射器,CHOICARE无菌一次性使用LDV注射器

K号: K213013 · 2022-09-19

决定日期2022-09-19
产品代码QNQ
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Jeil Tech Co., Ltd.. It received FDA 510(k) clearance on 2022-09-19 under 510(k) number K213013. The device is classified under product code QNQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?

Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe is a medical device that received FDA 510(k) clearance on 2022-09-19. The listed applicant is Jeil Tech Co., Ltd.. The 510(k) number is K213013.

When did Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe receive FDA 510(k) clearance?

Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe received FDA 510(k) clearance on 2022-09-19, under 510(k) number K213013.

Who is the listed applicant for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?

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

What is the FDA product code for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?

The FDA product code for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe is QNQ.

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:QNQ)

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

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