FDA 510(k)

輪廓24

K 號：K183111 · 2018-12-07

決定日期2018-12-07

產品代碼MOS

諮詢委員會RA

決定相當於

器材摘要

Contour 24 is the device name listed in this FDA 510(k) record. The listed applicant is Quality Electrodynamics, LLC. It received FDA 510(k) clearance on 2018-12-07 under 510(k) number K183111. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Contour 24?

Contour 24 is a medical device that received FDA 510(k) clearance on 2018-12-07. The listed applicant is Quality Electrodynamics, LLC. The 510(k) number is K183111.

When did Contour 24 receive FDA 510(k) clearance?

Contour 24 received FDA 510(k) clearance on 2018-12-07, under 510(k) number K183111.

Who is the listed applicant for Contour 24?

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

What is the FDA product code for Contour 24?

The FDA product code for Contour 24 is MOS.

其他以 Quality Electrodynamics, LLC 為申請人之記錄

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相關器械（代碼：MOS）

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官方來源

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