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CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001

Page Type
Cleared 510(K)
510(k) Number
K012241
510(k) Type
Traditional
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2002
Days to Decision
199 days
Submission Type
Summary

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001

Page Type
Cleared 510(K)
510(k) Number
K012241
510(k) Type
Traditional
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2002
Days to Decision
199 days
Submission Type
Summary