KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT

KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT is an FDA 510(k)-cleared medical device (K953980) manufactured by Kreuzer Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 15, 1995. Regulation: 8.