
Anthos Labtec Instruments
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ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III is an FDA 510(k)-cleared medical device (K931907) manufactured by Anthos Labtec Instruments. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 28, 1993. Regulation: 8.