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CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS

Page Type
Cleared 510(K)
510(k) Number
K894359
510(k) Type
Traditional
Applicant
HEMOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1989
Days to Decision
53 days

CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS

Page Type
Cleared 510(K)
510(k) Number
K894359
510(k) Type
Traditional
Applicant
HEMOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1989
Days to Decision
53 days