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EMORY CARDIAC TOOLBOX 3.2

Page Type
Cleared 510(K)
510(k) Number
K130902
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2013
Days to Decision
74 days
Submission Type
Summary

EMORY CARDIAC TOOLBOX 3.2

Page Type
Cleared 510(K)
510(k) Number
K130902
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2013
Days to Decision
74 days
Submission Type
Summary