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SCIMED(R) COURIER GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K946272
510(k) Type
Traditional
Applicant
SCIMED PERIPHERAL INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1995
Days to Decision
115 days
Submission Type
Summary

SCIMED(R) COURIER GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K946272
510(k) Type
Traditional
Applicant
SCIMED PERIPHERAL INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1995
Days to Decision
115 days
Submission Type
Summary