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RESUBMITTED MULTIORGAN PERFUSION CANNULA

Page Type
Cleared 510(K)
510(k) Number
K902394
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
120 days

RESUBMITTED MULTIORGAN PERFUSION CANNULA

Page Type
Cleared 510(K)
510(k) Number
K902394
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
120 days