
Gendron, Inc.
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REGENCY POWER WHEELCHAIR, MODEL 7200, 7500 & 7800 is an FDA 510(k)-cleared medical device (K001923) manufactured by Gendron, Inc.. 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 August 24, 2000. Regulation: 8.