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MODIFIED SIMPSON PERIPHERAL ATHEROCATH

Page Type
Cleared 510(K)
510(k) Number
K874706
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1988
Days to Decision
61 days

MODIFIED SIMPSON PERIPHERAL ATHEROCATH

Page Type
Cleared 510(K)
510(k) Number
K874706
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1988
Days to Decision
61 days