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KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002901
510(k) Type
Traditional
Applicant
The Kendall Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2001
Days to Decision
191 days
Submission Type
Summary

KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002901
510(k) Type
Traditional
Applicant
The Kendall Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2001
Days to Decision
191 days
Submission Type
Summary