Last synced on 14 November 2025 at 11:06 pm

BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K073434
510(k) Type
Special
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2008
Days to Decision
117 days
Submission Type
Summary

BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K073434
510(k) Type
Special
Applicant
BIPORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2008
Days to Decision
117 days
Submission Type
Summary