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DOUBLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K872248
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1987
Days to Decision
61 days

DOUBLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K872248
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1987
Days to Decision
61 days