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ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039

Page Type
Cleared 510(K)
510(k) Number
K082382
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2008
Days to Decision
115 days
Submission Type
Summary

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039

Page Type
Cleared 510(K)
510(k) Number
K082382
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2008
Days to Decision
115 days
Submission Type
Summary