SPATULA'S #'S 7618,7248,7240,7242,5108

SPATULA'S #'S 7618,7248,7240,7242,5108 is an FDA 510(k)-cleared medical device (K791983) 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.