BEDPAN, SINGLE PATIENT USE, TECNOL

BEDPAN, SINGLE PATIENT USE, TECNOL is an FDA 510(k)-cleared medical device (K760307) manufactured by Tecnol New Jersey Wound Care, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 10, 1976. Regulation: 8.