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CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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