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CARDIQ EXPRESS VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K073138
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2008
Days to Decision
111 days
Submission Type
Summary

CARDIQ EXPRESS VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K073138
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2008
Days to Decision
111 days
Submission Type
Summary