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CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052240
510(k) Type
Abbreviated
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2005
Days to Decision
63 days
Submission Type
Summary

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052240
510(k) Type
Abbreviated
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2005
Days to Decision
63 days
Submission Type
Summary