
Dynarex Corp.
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TOWEL DRAPE, MODELS 4409, 4410 is an FDA 510(k)-cleared medical device (K012957) manufactured by Dynarex Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 5, 2002. Regulation: 8.