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MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K081220
510(k) Type
Special
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2008
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K081220
510(k) Type
Special
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2008
Days to Decision
28 days
Submission Type
Summary