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GUIDING CATHETER (TIP SOFTNESS CHANGE)

Page Type
Cleared 510(K)
510(k) Number
K883981
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1988
Days to Decision
43 days

GUIDING CATHETER (TIP SOFTNESS CHANGE)

Page Type
Cleared 510(K)
510(k) Number
K883981
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1988
Days to Decision
43 days