Last synced on 25 January 2026 at 3:41 am

KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042461
510(k) Type
Abbreviated
Applicant
Kendall
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
91 days
Submission Type
Summary

KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042461
510(k) Type
Abbreviated
Applicant
Kendall
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
91 days
Submission Type
Summary