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MOME ECG CONTINUOUS DETECTION AND ARRHYTHMIA DETECTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133753
510(k) Type
Traditional
Applicant
Infobionic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2014
Days to Decision
284 days
Submission Type
Summary

MOME ECG CONTINUOUS DETECTION AND ARRHYTHMIA DETECTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133753
510(k) Type
Traditional
Applicant
Infobionic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2014
Days to Decision
284 days
Submission Type
Summary