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CORDIS ST STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K963214
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1996
Days to Decision
89 days
Submission Type
Summary

CORDIS ST STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K963214
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1996
Days to Decision
89 days
Submission Type
Summary