FDA 510(k)

InPen系统应用（MMT-8060（iOS），MMT-8061（Android））

K号: K242775 · 2024-11-12

决定日期2024-11-12

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

InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 2024-11-12 under 510(k) number K242775. 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 InPen System App (MMT-8060 (iOS), MMT-8061 (Android))?

InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) is a medical device that received FDA 510(k) clearance on 2024-11-12. The listed applicant is Medtronic Minimed. The 510(k) number is K242775.

When did InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) receive FDA 510(k) clearance?

InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) received FDA 510(k) clearance on 2024-11-12, under 510(k) number K242775.

Who is the listed applicant for InPen System App (MMT-8060 (iOS), MMT-8061 (Android))?

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

What is the FDA product code for InPen System App (MMT-8060 (iOS), MMT-8061 (Android))?

The FDA product code for InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) is NDC.

列明Medtronic Minimed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。

K261962SmartGuard技术；预测性低血糖技术 K253701SmartGuard技术；预测性低血糖技术 K253512MiniMed Go 应用 K241622扩展储液器；MiniMed储液器 K160860MiniMed Quick-serter

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。