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CORDIS STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K952067
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1995
Days to Decision
79 days
Submission Type
Summary

CORDIS STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K952067
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1995
Days to Decision
79 days
Submission Type
Summary