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FOCUS BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K952064
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1995
Days to Decision
50 days
Submission Type
Summary

FOCUS BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K952064
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1995
Days to Decision
50 days
Submission Type
Summary