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MICROTRACK

Page Type
Cleared 510(K)
510(k) Number
K935929
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1994
Days to Decision
87 days
Submission Type
Statement

MICROTRACK

Page Type
Cleared 510(K)
510(k) Number
K935929
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1994
Days to Decision
87 days
Submission Type
Statement