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ULTRAVERSE 014 AND 018 BALLOON DILATATION CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K093965
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
84 days
Submission Type
Summary

ULTRAVERSE 014 AND 018 BALLOON DILATATION CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K093965
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
84 days
Submission Type
Summary