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MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER

Page Type
Cleared 510(K)
510(k) Number
K023223
510(k) Type
Special
Applicant
LUMEND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2002
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER

Page Type
Cleared 510(K)
510(k) Number
K023223
510(k) Type
Special
Applicant
LUMEND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2002
Days to Decision
27 days
Submission Type
Summary