
Serral, S.A. DE C.V.
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SERRALAPG is an FDA 510(k)-cleared medical device (K033762) manufactured by Serral, S.A. DE C.V.. 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 14, 2004. Regulation: 8.