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DUAL LUMEN MIDLINE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K010349
510(k) Type
Special
Applicant
CATHETER INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2001
Days to Decision
23 days
Submission Type
Summary

DUAL LUMEN MIDLINE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K010349
510(k) Type
Special
Applicant
CATHETER INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2001
Days to Decision
23 days
Submission Type
Summary