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CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K914141
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1991
Days to Decision
37 days
Submission Type
Statement

CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K914141
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1991
Days to Decision
37 days
Submission Type
Statement