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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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