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COAGULATION CONTROL, LEVEL III

Page Type
Cleared 510(K)
510(k) Number
K870687
510(k) Type
Traditional
Applicant
U. S. DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
60 days

COAGULATION CONTROL, LEVEL III

Page Type
Cleared 510(K)
510(k) Number
K870687
510(k) Type
Traditional
Applicant
U. S. DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
60 days