TELEMETRY POWER PACK MODEL 2

TELEMETRY POWER PACK MODEL 2 is an FDA 510(k)-cleared medical device (K891927) manufactured by Lucas & Rhea Mfg.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 25, 1990. Regulation: 8.