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CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K973298
510(k) Type
Traditional
Applicant
CARDIMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1998
Days to Decision
297 days
Submission Type
Summary

CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K973298
510(k) Type
Traditional
Applicant
CARDIMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1998
Days to Decision
297 days
Submission Type
Summary