
Gunnell, Inc.
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REHAB TNT, REHAB RAM, REHAB MAC, REHAB KIDSTER, BARIATRIC REHAB TNT AND REHAB RAM is an FDA 510(k)-cleared medical device (K111636) manufactured by Gunnell, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 2, 2012. Regulation: 8.