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CORDIS STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K873403
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
211 days

CORDIS STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K873403
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
211 days