FDA 510(k)

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI

K 號：K173273 · 2017-11-09

決定日期2017-11-09

產品代碼MQB

諮詢委員會RA

決定相當於

器材摘要

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is the device name listed in this FDA 510(k) record. The listed applicant is Imaging Dynamics Company , Ltd.. It received FDA 510(k) clearance on 2017-11-09 under 510(k) number K173273. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Aquarius 8600 1417WCI; Aquarius 8600 1717WCI?

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Imaging Dynamics Company , Ltd.. The 510(k) number is K173273.

When did Aquarius 8600 1417WCI; Aquarius 8600 1717WCI receive FDA 510(k) clearance?

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI received FDA 510(k) clearance on 2017-11-09, under 510(k) number K173273.

Who is the listed applicant for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI?

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

What is the FDA product code for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI?

The FDA product code for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is MQB.

其他以 Imaging Dynamics Company , Ltd. 為申請人之記錄

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K171169Aquarius 8600 1417TG 及 Aquarius 8600 1717TG K171175Aquarius 8600 1417WC K170202Aquarius 8600

相關器械（代碼：MQB）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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