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)

Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles

K号: K171518 · 2018-01-05

决定日期2018-01-05
产品代码BSP
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Kindly Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2018-01-05 under 510(k) number K171518. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles?

Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles is a medical device that received FDA 510(k) clearance on 2018-01-05. The listed applicant is Zhejiang Kindly Medical Devices Co., Ltd.. The 510(k) number is K171518.

When did Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles receive FDA 510(k) clearance?

Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles received FDA 510(k) clearance on 2018-01-05, under 510(k) number K171518.

Who is the listed applicant for Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles?

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

What is the FDA product code for Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles?

The FDA product code for Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles is BSP.

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Zhejiang Kindly Medical Devices 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。

相关器械(代码:BSP)

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。

↑