STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000

STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000 is an FDA 510(k)-cleared medical device (K845023) manufactured by Storz Instrument Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 27, 1985. Regulation: 8.