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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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