FDA 510(k)

Magnesium

K号: K173294 · 2018-05-18

决定日期2018-05-18

产品代码JGJ

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

Magnesium is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2018-05-18 under 510(k) number K173294. The device is classified under product code JGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Magnesium?

Magnesium is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is Abbott Laboratories. The 510(k) number is K173294.

When did Magnesium receive FDA 510(k) clearance?

Magnesium received FDA 510(k) clearance on 2018-05-18, under 510(k) number K173294.

Who is the listed applicant for Magnesium?

FDA 510(k)记录显示，申请人为阿伯特实验室。这本身并不能确立该设备的制造商。

What is the FDA product code for Magnesium?

The FDA product code for Magnesium is JGJ.

列明Abbott Laboratories为申报人的其他记录

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