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Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181208
510(k) Type
Traditional
Applicant
Vygon USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2018
Days to Decision
179 days
Submission Type
Summary

Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181208
510(k) Type
Traditional
Applicant
Vygon USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2018
Days to Decision
179 days
Submission Type
Summary