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SCIMED ENTRE II PTCA GUIDE WIRE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K935022
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
90 days
Submission Type
Summary

SCIMED ENTRE II PTCA GUIDE WIRE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K935022
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
90 days
Submission Type
Summary