DUS-7000 Digital Color Doppler Ultrasound System

FDA 510(k) K172055 · Advanced Instrumentations, Inc.

Substantially Equivalent

510(k) numberK172055

Submission

Device name
DUS-7000 Digital Color Doppler Ultrasound System
Applicant
Advanced Instrumentations, Inc.
Miami, FL, US
Received
July 6, 2017
Decision date
August 31, 2017
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IYN – System, Imaging, Pulsed Doppler, Ultrasonic
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1550
Specialty
Radiology

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K261412V8/XV8/XH8/H8/cV8/V8 ONE/XV8 ONE/XH8 ONE/H8 ONE/cV8 ONE Diagnostic Ultrasound System…IYN · Traditional Samsung Medison Co., Ltd.07/28/2026SE
K261211Philips EPIQ Series Diagnostic Ultrasound System; Philips Affiniti Series Diagnostic…IYN · Traditional Philips Ultrasound, LLC07/27/2026SE
K261272ePascal S/ ePascal SOR/ ePascal S5/ ePascal SA/ ePascal SE/ ePascal 80Elite/ ePascal 80/…IYN · Traditional Esonic Technology (Wuhan) Co., Ltd.07/23/2026SE
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More from Beijing Konted Medical Technology Co.,Ltd

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K172931DUS-6000 Digital Ultrasonic Diagnostic Imaging SystemIYO · Abbreviated 12/01/2017SE
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K132077Patient MonitorMHX · Traditional 04/23/2014SE
K132059Diagnostic Ultrasound SystemIYN · Traditional 10/25/2013SE
K123048Patient Monitor Models PM-2000A, PM-2000A+, PM-2000A ProMHX · Traditional 01/11/2013SE
K120075AM-6000 Anesthesia MachineBSZ · Traditional 01/26/2012SE
K112317FM-9000 Plus Fetal and Maternal MonitorHGM · Traditional 12/21/2011SE
K112529TD-5000 & TD-6000 Ultrasonic Tabletop DopplerKNG · Traditional 10/27/2011SE
K112022DUS-3000/DUS-3000PLUS Digital Ultrasonic Diagnostic Imaging SystemIYO · Traditional 09/22/2011SE
K111934PD-100 Series Ultrasonic Pocket DopplerKNG · Traditional 09/22/2011SE

Questions and answers

When was DUS-7000 Digital Color Doppler Ultrasound System cleared by the FDA?

DUS-7000 Digital Color Doppler Ultrasound System (K172055) received a 510(k) decision of Substantially Equivalent on August 31, 2017, 56 days after the submission was received.

What is the product code of K172055?

The FDA product code is IYN – System, Imaging, Pulsed Doppler, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 892.1550.