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INTRODUCING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883933
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1988
Days to Decision
78 days

INTRODUCING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883933
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1988
Days to Decision
78 days