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ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2155-XXYY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101735
510(k) Type
Special
Applicant
Angioscore, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2010
Days to Decision
23 days
Submission Type
Summary

ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2155-XXYY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101735
510(k) Type
Special
Applicant
Angioscore, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2010
Days to Decision
23 days
Submission Type
Summary