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SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL

Page Type
Cleared 510(K)
510(k) Number
K922410
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1992
Days to Decision
63 days
Submission Type
Summary

SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL

Page Type
Cleared 510(K)
510(k) Number
K922410
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1992
Days to Decision
63 days
Submission Type
Summary