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CARDIMA TRACKER(R) INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K932800
510(k) Type
Traditional
Applicant
CARDIMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1993
Days to Decision
195 days
Submission Type
Summary

CARDIMA TRACKER(R) INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K932800
510(k) Type
Traditional
Applicant
CARDIMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1993
Days to Decision
195 days
Submission Type
Summary