
Synectics-Dantec
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ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF. is an FDA 510(k)-cleared medical device (K925405) manufactured by Synectics-Dantec. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 29, 1994. Regulation: 8.