
Edward Weck, Inc.
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TOME'S #'S 1221,1222,1223,1314,6640,6642 is an FDA 510(k)-cleared medical device (K791980) manufactured by Edward Weck, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 3, 1979. Regulation: 8.

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