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FIRST MIDCATH CATHETER WITH DUAL LUMENS

Page Type
Cleared 510(K)
510(k) Number
K964049
510(k) Type
Traditional
Applicant
BECTON DICKINSON VASCULAR ACCESS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1997
Days to Decision
89 days
Submission Type
Summary

FIRST MIDCATH CATHETER WITH DUAL LUMENS

Page Type
Cleared 510(K)
510(k) Number
K964049
510(k) Type
Traditional
Applicant
BECTON DICKINSON VASCULAR ACCESS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1997
Days to Decision
89 days
Submission Type
Summary