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KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
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)
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