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ANGIOSCULPT SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K050629
510(k) Type
Traditional
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
175 days
Submission Type
Summary

ANGIOSCULPT SCORING BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K050629
510(k) Type
Traditional
Applicant
ANGIOSCORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
175 days
Submission Type
Summary