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ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039

Page Type
Cleared 510(K)
510(k) Number
K080151
510(k) Type
Traditional
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2008
Days to Decision
94 days
Submission Type
Summary

ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039

Page Type
Cleared 510(K)
510(k) Number
K080151
510(k) Type
Traditional
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2008
Days to Decision
94 days
Submission Type
Summary