DM-3000 Digital Blood Pressure Monitor

FDA 510(k) K061086 · Nihon Seimitsu Sokki Co., Ltd.

Substantially Equivalent

510(k) numberK061086

Submission

Device name
DM-3000 Digital Blood Pressure Monitor
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Mount Dora, FL, US
Received
April 18, 2006
Decision date
August 10, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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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K050697Model DS-1901 Digital Blood Pressure MonitorDXN · Traditional 03/25/2005SE
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Questions and answers

When was DM-3000 Digital Blood Pressure Monitor cleared by the FDA?

DM-3000 Digital Blood Pressure Monitor (K061086) received a 510(k) decision of Substantially Equivalent on August 10, 2006, 114 days after the submission was received.

What is the product code of K061086?

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