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LEMAITRE BILIARY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992941
510(k) Type
Traditional
Applicant
VASCUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
134 days
Submission Type
Statement

LEMAITRE BILIARY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992941
510(k) Type
Traditional
Applicant
VASCUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
134 days
Submission Type
Statement