Doppler Imaging Option

FDA 510(k) K840140 · Hewlett-Packard Co.

Substantially Equivalent

510(k) numberK840140

Submission

Device name
Doppler Imaging Option
Applicant
Hewlett-Packard Co.
Walker, MI, US
Received
January 4, 1984
Decision date
August 23, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

Other 510(k)s with product code IYN

510(k)DeviceApplicantDecision
K261313Vivid Explorer/Vivid Advanced/Vivid FocusIYN · Traditional GE Medical Systems Ultrasound and Primary Care…09/02/2026SE
K254027Digital Color Doppler Ultrasound System (Marvo 95/Marvo 95 Elite/Marvo 90/Marvo 90…IYN · Traditional Sonoscape Medical Corp.08/24/2026SE
K261668Venue GoIYN · Traditional GE Medical Systems Ultrasound and Primary care…08/07/2026SE
K262311Alturion Series Diagnostic Ultrasound SystemIYN · Special Philips Ultrasound, LLC08/04/2026SE
K261835LOGIQ FocusIYN · Traditional GE Medical Systems Ultrasound and Primary Care…07/30/2026SE
K261288Handheld Ultrasound ScannerIYN · Traditional Imgfax Co., Ltd.07/30/2026SE
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
K261081Pocket Ultrasound System (C10MTpro,C10MXpro,C10MSpro,C10MBpro,C10MRpro)IYN · Special Beijing Konted Medical Technology Co.,Ltd07/23/2026SE

More from Beijing Konted Medical Technology Co.,Ltd

510(k)DeviceDecision
K992543Heartstream XLT Defibrillator/Monitor, Ac Charger, DC Charger, Data Card, Single Bay…MKJ · Traditional 05/18/2000SE
K993383HP Viridia Multi-Measurement Server/Compact Portable Patient Monitor Models M3000A…DSI · Abbreviated 02/03/2000SE
K992273HP Viridia Multi-Measurement Server/Compact Portable Patient Monitor…MHX · Abbreviated 01/28/2000SE
K993587HP M2376A Device Link SystemMQS · Traditional 01/20/2000SE
K993169Modification of: Physiological Signal Transmitter and Receiver, Model 3810ADRG · Traditional 12/20/1999SE
K992595HP Viridia Component Monitoring System, Model Rev. K with Easi-St Segment Measurement…MHX · Special 12/08/1999SE
K992977Hewlett Packard Multifunction Pediatric Defib Function, Model M3503A & M3504AMKJ · Traditional 12/01/1999SE
K993516HP M2600A Viridia Telemetry SystemDSI · Special 11/08/1999SE
K992674HP Viridia CMS Patient Monitor with EEG Parameter, Model M1027AMHX · Abbreviated 11/08/1999SE
K993171HP Viridia Information System, Models M3150A/ M3151A/ M3153A/ M3154ADSI · Special 10/21/1999SE

Questions and answers

When was Doppler Imaging Option cleared by the FDA?

Doppler Imaging Option (K840140) received a 510(k) decision of Substantially Equivalent on August 23, 1984, 232 days after the submission was received.

What is the product code of K840140?

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