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SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F

Page Type
Cleared 510(K)
510(k) Number
K883346
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1988
Days to Decision
60 days

SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F

Page Type
Cleared 510(K)
510(k) Number
K883346
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1988
Days to Decision
60 days