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CONDUCTION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K031600
510(k) Type
Traditional
Applicant
MICOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2003
Days to Decision
84 days
Submission Type
Summary

CONDUCTION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K031600
510(k) Type
Traditional
Applicant
MICOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2003
Days to Decision
84 days
Submission Type
Summary