Oregon Scintific

FDA 510(k) K131245 · Idt Technology Limited

Substantially Equivalent

510(k) numberK131245

Submission

Device name
Oregon Scintific
Applicant
Idt Technology Limited
Shenzhen,, CN
Received
May 1, 2013
Decision date
January 17, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DXN – System, Measurement, Blood-Pressure, Non-Invasive
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1130
Specialty
Cardiovascular

Other 510(k)s with product code DXN

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K261929Upper Arm Blood pressure monitor (BP7155D)DXN · Special OMRON Healthcare, Inc.09/10/2026SE
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K262658Automatic Digital Blood Pressure monitor (LD-526)DXN · Special Honsun (Nantong) Co., Ltd.08/31/2026SE
K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus…DXN · Traditional JOYTECH Healthcare Co., Ltd.08/26/2026SE
K261061BP Go (BPP-855)DXN · Traditional Wellvii, Inc.08/13/2026SE
K253425Arm-type Fully Automatic Digital Blood Pressure Monitor…DXN · Traditional Joytech Healthcare Co. , Ltd.08/13/2026SE
K261136Blood Pressure Monitor (M501,M501A,M502,M502A,M502C,M502D)DXN · Traditional Guangzhou Daxin Health Technology Co., Ltd.07/23/2026SE
K261082Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)DXN · Traditional Microlife Corporation07/23/2026SE
K253126Wrist Blood Pressure Monitor (XW-05)DXN · Traditional Shenzhen Ziqing Medical Equipment Co., Ltd.06/18/2026SE
K260693VicorderCS (VCS-SYS-1100)DXN · Traditional 80 Beats Medical GmbH06/16/2026SE

More from 80 Beats Medical GmbH

510(k)DeviceDecision
K151415Oregon ScientificDXN · Traditional 10/21/2015SE
K050083Blood-Pressure Meter, BPW120DXN · Traditional 04/08/2005SE
K031167High Precision Body Weight Monitor with Body Fat IndexMNW · Traditional 01/28/2004SE
K020433FT101 Forehead Thermometer; FT101 Infrared Digital ThermometerFLL · Traditional 07/11/2002SE
K021252Blood-Pressure MeterDXN · Traditional 06/17/2002SE

Questions and answers

When was Oregon Scintific cleared by the FDA?

Oregon Scintific (K131245) received a 510(k) decision of Substantially Equivalent on January 17, 2014, 261 days after the submission was received.

What is the product code of K131245?

The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.