
Meditec, Inc.
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MDS-83 IN DERMATOLOGICAL/PLASTIC SURGERY APPLICATI is an FDA 510(k)-cleared medical device (K854833) manufactured by Meditec, 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 April 3, 1986. Regulation: 8.