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FDA 510(k) Applications Submitted by INFOBIONIC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K133753
12/09/2013
MOME ECG CONTINUOUS DETECTION AND ARRHYTHMIA DETECTOR
INFOBIONIC, INC.
K230265
01/31/2023
MoMe« ARC Wireless Ambulatory ECG Monitoring and Detection System
InfoBionic, Inc.
K152491
09/01/2015
MoMe Software Platform
INFOBIONIC, INC.
K160064
01/13/2016
MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System
INFOBIONIC, INC.
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