Upper Arm Blood pressure monitor (BP7155D)

FDA 510(k) K261929 · OMRON Healthcare, Inc.

Substantially Equivalent

510(k) numberK261929

Submission

Device name
Upper Arm Blood pressure monitor (BP7155D)
Applicant
OMRON Healthcare, Inc.
Hoffman Estates, IL, US
Received
June 9, 2026
Decision date
September 10, 2026
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 Upper Arm Blood pressure monitor (BP7155D) cleared by the FDA?

Upper Arm Blood pressure monitor (BP7155D) (K261929) received a 510(k) decision of Substantially Equivalent on September 10, 2026, 93 days after the submission was received.

What is the product code of K261929?

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