Arm Automatic Blood Pressure Monitor

FDA 510(k) K130325 · Shenzhen Pump Medical System Co., Ltd.

Substantially Equivalent

510(k) numberK130325

Submission

Device name
Arm Automatic Blood Pressure Monitor
Applicant
Shenzhen Pump Medical System Co., Ltd.
Shenzhen, Guangdong, CN
Received
February 8, 2013
Decision date
December 24, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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

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More from 80 Beats Medical GmbH

510(k)DeviceDecision
K161712Arm automatic blood pressure monitorDXN · Special 04/05/2017SE
K161708Arm automatic blood pressure monitorDXN · Special 11/22/2016SE
K151258Arm automatic blood pressure monitorDXN · Special 02/18/2016SE
K151810Bpump Blood Pressure CuffDXQ · Traditional 12/17/2015SE
K141416Blood Pressure MonitorDXN · Traditional 10/09/2014SE
K131210Electronic ThermometerFLL · Traditional 03/18/2014SE

Questions and answers

When was Arm Automatic Blood Pressure Monitor cleared by the FDA?

Arm Automatic Blood Pressure Monitor (K130325) received a 510(k) decision of Substantially Equivalent on December 24, 2013, 319 days after the submission was received.

What is the product code of K130325?

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