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CENTRAL VENOUS ACCESS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901701
510(k) Type
Traditional
Applicant
CARDIOPULMONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1990
Days to Decision
160 days

CENTRAL VENOUS ACCESS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901701
510(k) Type
Traditional
Applicant
CARDIOPULMONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1990
Days to Decision
160 days