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C-DAK DUO-FLUX ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
510(k) Number
K811830
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1981
Days to Decision
84 days

C-DAK DUO-FLUX ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
510(k) Number
K811830
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1981
Days to Decision
84 days