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FDA 510(k)

FreeStyle Libre 2闪式血糖监测系统

K号: K211102 · 2021-08-11

决定日期2021-08-11
产品代码QLG
咨询委员会CH 请注意,您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本,以便我能够进行准确的翻译。
决定实质等同

器械摘要

FreeStyle Libre 2 Flash Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Diabetes Care, Inc.. It received FDA 510(k) clearance on 2021-08-11 under 510(k) number K211102. The device is classified under product code QLG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FreeStyle Libre 2 Flash Glucose Monitoring System?

FreeStyle Libre 2 Flash Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2021-08-11. The listed applicant is Abbott Diabetes Care, Inc.. The 510(k) number is K211102.

When did FreeStyle Libre 2 Flash Glucose Monitoring System receive FDA 510(k) clearance?

FreeStyle Libre 2 Flash Glucose Monitoring System received FDA 510(k) clearance on 2021-08-11, under 510(k) number K211102.

Who is the listed applicant for FreeStyle Libre 2 Flash Glucose Monitoring System?

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

What is the FDA product code for FreeStyle Libre 2 Flash Glucose Monitoring System?

The FDA product code for FreeStyle Libre 2 Flash Glucose Monitoring System is QLG.

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列明Abbott Diabetes Care, Inc.为申报人的其他记录

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相关器械(代码:QLG)

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官方来源

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