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MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130725
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2013
Days to Decision
30 days
Submission Type
Summary

MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130725
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2013
Days to Decision
30 days
Submission Type
Summary