
Customed, Inc.
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FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633 is an FDA 510(k)-cleared medical device (K974647) manufactured by Customed, Inc.. 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 January 4, 1998. Regulation: 8.