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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