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Needle Tech Products, Inc.
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NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013 is an FDA 510(k)-cleared medical device (K031173) manufactured by Needle Tech Products, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 22, 2003. Regulation: 8.