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BIPORE BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K961980
510(k) Type
Traditional
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1996
Days to Decision
115 days
Submission Type
Summary

BIPORE BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K961980
510(k) Type
Traditional
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1996
Days to Decision
115 days
Submission Type
Summary