
CIVCO Medical Instruments Co., Inc.
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TRANS/R - FP(3) is an FDA 510(k)-cleared medical device (K900016) manufactured by CIVCO Medical Instruments Co., Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 10, 1990. Regulation: 8.