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FDA 510(k)

LiverMultiScan

K号: K202170 · 2020-10-02

决定日期2020-10-02
产品代码LNH
咨询委员会RA
决定实质等同

器械摘要

LiverMultiScan is the device name listed in this FDA 510(k) record. The listed applicant is Perspectum, Ltd.. It received FDA 510(k) clearance on 2020-10-02 under 510(k) number K202170. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LiverMultiScan?

LiverMultiScan is a medical device that received FDA 510(k) clearance on 2020-10-02. The listed applicant is Perspectum, Ltd.. The 510(k) number is K202170.

When did LiverMultiScan receive FDA 510(k) clearance?

LiverMultiScan received FDA 510(k) clearance on 2020-10-02, under 510(k) number K202170.

Who is the listed applicant for LiverMultiScan?

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

What is the FDA product code for LiverMultiScan?

The FDA product code for LiverMultiScan is LNH.

相关临床试验

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列明Perspectum, Ltd.为申报人的其他记录

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相关器械(代码:LNH)

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官方来源

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