
Medical Device Resource Corp.
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LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 is an FDA 510(k)-cleared medical device (K092284) manufactured by Medical Device Resource Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 31, 2009. Regulation: 8.