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CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K892530
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1989
Days to Decision
168 days

CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K892530
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1989
Days to Decision
168 days