
Mobilife, LLC
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MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR is an FDA 510(k)-cleared medical device (K061116) manufactured by Mobilife, LLC. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 2, 2006. Regulation: 8.