FDA UDI In Commercial Distribution 🇺🇸 United States

Samsung ECG Monitor App with Irregular Heart Rhythm Notification

DI: 08806094940763 · Model: 1.X · Samsung Electronics Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Samsung ECG Monitor App with Irregular Heart Rhythm Notification
Primary DI
08806094940763
Version / Model
1.X
Company Name
Samsung Electronics Co., Ltd.
Labeler DUNS
687967554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-23
Public Version
2
Public Version Date
2024-07-15
Public Version Status
Update
Public Device Record Key
79a20584-8685-457e-b26e-6d90dca27cf7

Device Description

The Samsung ECG Monitor Application with Irregular Heart Rhythm Notification is an over-the-counter (OTC) software-only, mobile medical application operating on a compatible Samsung Galaxy Watch and Phone for informational use only in adults 22 years and older. The app analyzes pulse rate data to identify episodes of irregular heart rhythms suggestive of atrial fibrillation (AFib) and provides a notification suggesting the user record an ECG to analyze the heart rhythm. The Irregular Heart Rhythm Notification Feature is not intended to provide a notification on every episode of irregular rhythm suggestive of AFib and the absence of a notification is not intended to indicate no disease process is present; rather the feature is intended to opportunistically acquire pulse rate data when the user is still and analyze the data when determined sufficient toward surfacing a notification.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QDA Electrocardiograph Software For Over-The-Counter Use
QDB Photoplethysmograph Analysis Software For Over-The-Counter Use

GMDN Terms

Code Name
58884 Self-care monitoring/reporting software

Identifiers

Type ID
Primary 08806094940763

Premarket Submissions

Submission Number Supplement Number
K230292 000