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CORDIS REFLEX STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K905423
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1991
Days to Decision
87 days

CORDIS REFLEX STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K905423
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1991
Days to Decision
87 days