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BIOPORE BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K041293
510(k) Type
Abbreviated
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2004
Days to Decision
56 days
Submission Type
Summary

BIOPORE BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K041293
510(k) Type
Abbreviated
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2004
Days to Decision
56 days
Submission Type
Summary