Aquarius 8600 1417WCI; Aquarius 8600 1717WCI— 510(k) K173273

Name: FDA 510(k) clearance K173273
Creator: U.S. Food and Drug Administration
Published: 2017-11-09

Substantially Equivalent

Imaging Dynamics Company , Ltd.

FDA 510(k) clearance K173273 for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI, Substantially Equivalent on 2017-11-09. Applicant: Imaging Dynamics Company , Ltd.. Device class: 2.

Clearance details

Applicant: Imaging Dynamics Company , Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2017-10-12
Decision date: 2017-11-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Calgary, CA

Download summary PDF View on FDA.gov ↗

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