Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)

FDA 510(k) K252389 · Smwmed, Inc.

Substantially Equivalent

510(k) numberK252389

Submission

Device name
Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)
Applicant
Smwmed, Inc.
San Diego, CA, US
Received
July 31, 2025
Decision date
April 23, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DSH – Recorder, Magnetic Tape, Medical
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2800
Specialty
Cardiovascular

Other 510(k)s with product code DSH

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K260157LifeLens Physiological MonitorDSH · Traditional LifeLens Technologies, Inc.07/09/2026SE
K253293VitaloJAK Clinic (Model 7100)DSH · Special Vitalograph , Ltd.12/03/2025SE
K243650Zio® monitor (DFG0001)DSH · Traditional iRhythm Technologies, Inc.08/15/2025SE
K243603AeviceMDDSH · Traditional Aevice Health Pte. , Ltd.05/05/2025SE
K242583AT-Patch (ATP-C130/ATP-C70)DSH · Traditional Atsens Co., Ltd.05/02/2025SE
K232670HiCardi+ H100DSH · Traditional MEZOO Co., Ltd.09/20/2024SE
K233906S-Patch (S-Patch ExL)DSH · Special Wellysis Corp.02/16/2024SE
K231104ABPMproDSH · Traditional Somnomedics GmbH11/27/2023SE
K233110Carnation Ambulatory MonitorDSH · Traditional Bardy Diagnostics, Inc.11/22/2023SE
K230184Holter ECG and ABP SystemDSH · Traditional Edan Instruments, Inc.09/25/2023SE

Questions and answers

When was Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX) cleared by the FDA?

Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX) (K252389) received a 510(k) decision of Substantially Equivalent on April 23, 2026, 266 days after the submission was received.

What is the product code of K252389?

The FDA product code is DSH – Recorder, Magnetic Tape, Medical, a Class II (moderate risk) device regulated under 21 CFR 870.2800.