FDA 510(k)

t:slim X2 胰岛素泵（带互操作性技术，含 t:connect 移动应用程序）

K号: K203234 · 2022-02-15

决定日期2022-02-15

产品代码QFG

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决定实质等同

器械摘要

t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) is the device name listed in this FDA 510(k) record. The listed applicant is Tandem Diabetes Care, Inc.. It received FDA 510(k) clearance on 2022-02-15 under 510(k) number K203234. The device is classified under product code QFG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app)?

t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) is a medical device that received FDA 510(k) clearance on 2022-02-15. The listed applicant is Tandem Diabetes Care, Inc.. The 510(k) number is K203234.

When did t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) receive FDA 510(k) clearance?

t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) received FDA 510(k) clearance on 2022-02-15, under 510(k) number K203234.

Who is the listed applicant for t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app)?

The FDA 510(k) record lists Tandem Diabetes Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app)?

The FDA product code for t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) is QFG.

列明Tandem Diabetes Care, Inc.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。

K260429Control-IQ+ 技术 K253074Tandem Mobi 胰岛素泵，具有互操作性技术 K250792t:slim X2 胰岛素泵，具备互操作性技术 K250798Control-IQ+ 技术 K243823Control-IQ+ 技术 K241078Tandem Mobi 胰岛素泵，具有互操作性技术

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官方来源

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