
Grass-Telefactor Product Group
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BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING is an FDA 510(k)-cleared medical device (K884937) manufactured by Grass-Telefactor Product Group. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 13, 1989. Regulation: 8.