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CARDIOX FLOW DETECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122400
510(k) Type
Traditional
Applicant
CARDIOX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2013
Days to Decision
455 days
Submission Type
Summary

CARDIOX FLOW DETECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122400
510(k) Type
Traditional
Applicant
CARDIOX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2013
Days to Decision
455 days
Submission Type
Summary