
3M Company
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3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX is an FDA 510(k)-cleared medical device (K874086) manufactured by 3M Company. 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 December 16, 1987. Regulation: 8.