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)

SureForm 45,SureForm 45 重装

K号: K183224 · 2019-01-18

决定日期2019-01-18
产品代码NAY
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

SureForm 45, SureForm 45 Reloads is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical. It received FDA 510(k) clearance on 2019-01-18 under 510(k) number K183224. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SureForm 45, SureForm 45 Reloads?

SureForm 45, SureForm 45 Reloads is a medical device that received FDA 510(k) clearance on 2019-01-18. The listed applicant is Intuitive Surgical. The 510(k) number is K183224.

When did SureForm 45, SureForm 45 Reloads receive FDA 510(k) clearance?

SureForm 45, SureForm 45 Reloads received FDA 510(k) clearance on 2019-01-18, under 510(k) number K183224.

Who is the listed applicant for SureForm 45, SureForm 45 Reloads?

The FDA 510(k) record lists Intuitive Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SureForm 45, SureForm 45 Reloads?

The FDA product code for SureForm 45, SureForm 45 Reloads is NAY.

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Intuitive Surgical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 14 个设备 →

相关器械(代码:NAY)

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。

↑