Microlife Upper Arm Automatic Digital Blood Pressure Monitor

FDA 510(k) K131346 · Microlife Intellectual Property GmbH

Substantially Equivalent

510(k) numberK131346

Submission

Device name
Microlife Upper Arm Automatic Digital Blood Pressure Monitor
Applicant
Microlife Intellectual Property GmbH
Great Neck, NY, US
Received
May 9, 2013
Decision date
June 6, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 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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Questions and answers

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

Microlife Upper Arm Automatic Digital Blood Pressure Monitor (K131346) received a 510(k) decision of Substantially Equivalent on June 6, 2013, 28 days after the submission was received.

What is the product code of K131346?

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