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CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063222
510(k) Type
Special
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2006
Days to Decision
21 days
Submission Type
Summary

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063222
510(k) Type
Special
Applicant
CARDIONET, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2006
Days to Decision
21 days
Submission Type
Summary