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LIFESITE HEMODIALYSIS ACCESS SYSTEM, CANNULA EXCHANGE KIT, INSERTION KIT, ACCESS CANNILA

Page Type
Cleared 510(K)
510(k) Number
K023023
510(k) Type
Traditional
Applicant
VASCA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2003
Days to Decision
449 days
Submission Type
Summary

LIFESITE HEMODIALYSIS ACCESS SYSTEM, CANNULA EXCHANGE KIT, INSERTION KIT, ACCESS CANNILA

Page Type
Cleared 510(K)
510(k) Number
K023023
510(k) Type
Traditional
Applicant
VASCA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2003
Days to Decision
449 days
Submission Type
Summary