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CARDIOX FLOW DETECTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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