SIGMA PEROXIDASE MYELOPEROXIDASE STAINING PROCEDUR

SIGMA PEROXIDASE MYELOPEROXIDASE STAINING PROCEDUR is an FDA 510(k)-cleared medical device (K844402) manufactured by Sigma Chemical Co.. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 3, 1985. Regulation: 8.