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CARDIOVENTION CORX SYSTEM, MODEL FG 0001

Page Type
Cleared 510(K)
510(k) Number
K012325
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2002
Days to Decision
260 days
Submission Type
Summary

CARDIOVENTION CORX SYSTEM, MODEL FG 0001

Page Type
Cleared 510(K)
510(k) Number
K012325
510(k) Type
Traditional
Applicant
CARDIOVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2002
Days to Decision
260 days
Submission Type
Summary