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HEMOCUE HEMOGLOBIN CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K882600
510(k) Type
Traditional
Applicant
REACT AND CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
24 days

HEMOCUE HEMOGLOBIN CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K882600
510(k) Type
Traditional
Applicant
REACT AND CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
24 days