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MODIFIED VAS-CATH CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890099
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/11/1989
Days to Decision
91 days

MODIFIED VAS-CATH CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890099
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/11/1989
Days to Decision
91 days