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ANGIOSCULPT PTA SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112182
510(k) Type
Special
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2011
Days to Decision
29 days
Submission Type
Summary

ANGIOSCULPT PTA SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112182
510(k) Type
Special
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2011
Days to Decision
29 days
Submission Type
Summary