Sensor, glucose, invasive
PMA编号：P150021 · 2026-09-01
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决定日期2026-09-01
PMA 编号P150021
产品代码MDS
设备分类第3类
医疗专科U
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。
器械摘要
Sensor, glucose, invasive 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 2026-09-01. The device is classified under product code MDS. It was reviewed by the CH advisory panel.
常见问题
What is the Sensor, glucose, invasive?
Sensor, glucose, invasive is a medical device that received FDA 510(k) clearance on 2026-09-01. The listed applicant is Abbott Diabetes Care, Inc..
When did Sensor, glucose, invasive receive FDA 510(k) clearance?
The clearance date for Sensor, glucose, invasive can be found in the official FDA records.
Sensor,葡萄糖，侵入式产品的列名申请人是谁？
The FDA 510(k) record lists Abbott Diabetes Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
什么是Sensor，葡萄糖，侵入式产品的FDA产品代码？
FDA产品代码为Sensor，葡萄糖，侵入式的是MDS。
相关临床试验
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官方来源
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