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DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892926
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/5/1989
Days to Decision
228 days

DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892926
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/5/1989
Days to Decision
228 days