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SCIMED TRANSEND EX STEERABLE GUIDE WIRE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K934122
510(k) Type
Traditional
Applicant
SCIMED PERIPHERAL INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1993
Days to Decision
43 days
Submission Type
Summary

SCIMED TRANSEND EX STEERABLE GUIDE WIRE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K934122
510(k) Type
Traditional
Applicant
SCIMED PERIPHERAL INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1993
Days to Decision
43 days
Submission Type
Summary