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)

Insulia糖尿病管理伴侣

K号: K172177 · 2017-11-07

申请人Voluntis Sa.
决定日期2017-11-07
产品代码NDC
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

Insulia Diabetes Management Companion is the device name listed in this FDA 510(k) record. The listed applicant is Voluntis Sa.. It received FDA 510(k) clearance on 2017-11-07 under 510(k) number K172177. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Insulia Diabetes Management Companion?

Insulia Diabetes Management Companion is a medical device that received FDA 510(k) clearance on 2017-11-07. The listed applicant is Voluntis Sa.. The 510(k) number is K172177.

When did Insulia Diabetes Management Companion receive FDA 510(k) clearance?

Insulia Diabetes Management Companion received FDA 510(k) clearance on 2017-11-07, under 510(k) number K172177.

Who is the listed applicant for Insulia Diabetes Management Companion?

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

What is the FDA product code for Insulia Diabetes Management Companion?

The FDA product code for Insulia Diabetes Management Companion is NDC.

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Voluntis Sa.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:NDC)

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。

↑