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FOCUS BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K944016
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
126 days
Submission Type
Summary

FOCUS BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K944016
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
126 days
Submission Type
Summary