FDA 510(k), K955300, TOTAL BILIRUBIN PROCEDURE
FDA 510(k), K955300, TOTAL BILIRUBIN PROCEDURE
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510(K) Number: K955300
Device Name: TOTAL BILIRUBIN PROCEDURE
Manufacturer:
Device Classification Name: Diazo Colorimetry, Bilirubin
Regulation Number: 862.1110
Classification Product Code: CIG
Date Received: 11/20/1995
Decision Date: 12/20/1995
Regulation Medical Specialty: Clinical Chemistry
Device Name: TOTAL BILIRUBIN PROCEDURE
Manufacturer:
Device Classification Name: Diazo Colorimetry, Bilirubin
Regulation Number: 862.1110
Classification Product Code: CIG
Date Received: 11/20/1995
Decision Date: 12/20/1995
Regulation Medical Specialty: Clinical Chemistry