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ANGIOTECH CVC

Page Type
Cleared 510(K)
510(k) Number
K073520
510(k) Type
Traditional
Applicant
ANGIOTECH PHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2008
Days to Decision
119 days
Submission Type
Summary

ANGIOTECH CVC

Page Type
Cleared 510(K)
510(k) Number
K073520
510(k) Type
Traditional
Applicant
ANGIOTECH PHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2008
Days to Decision
119 days
Submission Type
Summary