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Arvik Enterprises/ Mini Lap Technologies
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ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT is an FDA 510(k)-cleared medical device (K102274) manufactured by Arvik Enterprises/ Mini Lap Technologies. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 14, 2011. Regulation: 8.