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BIOPORE BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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