Last synced on 14 November 2025 at 11:06 pm

CORDIS 5.2 FRENCH SUPER TORQUE PLUS CARDIO CATH

Page Type
Cleared 510(K)
510(k) Number
K914007
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1991
Days to Decision
39 days
Submission Type
Statement

CORDIS 5.2 FRENCH SUPER TORQUE PLUS CARDIO CATH

Page Type
Cleared 510(K)
510(k) Number
K914007
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1991
Days to Decision
39 days
Submission Type
Statement