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VYGON 2 FR EPICUTANEO PUR-CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993052
510(k) Type
Traditional
Applicant
Vygon Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2000
Days to Decision
325 days
Submission Type
Statement

VYGON 2 FR EPICUTANEO PUR-CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993052
510(k) Type
Traditional
Applicant
Vygon Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2000
Days to Decision
325 days
Submission Type
Statement