
Turbo Wheelchair Co., Inc.
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MERLEXI CRAFT SERIES OF MANUAL (MECHANICAL) WHEELCHAIRS is an FDA 510(k)-cleared medical device (K032731) manufactured by Turbo Wheelchair Co., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 29, 2003. Regulation: 8.