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CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200

Page Type
Cleared 510(K)
510(k) Number
K032068
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
50 days
Submission Type
Summary

CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200

Page Type
Cleared 510(K)
510(k) Number
K032068
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
50 days
Submission Type
Summary