
Surgi-Med, Inc.
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PARAGON 9000 TILT AND TURN BED is an FDA 510(k)-cleared medical device (K872923) manufactured by Surgi-Med, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 13, 1987. Regulation: 8.

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