
Aspen Laboratories, Inc.
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ELECTROSURGICAL DISPERSIVE PLATE is an FDA 510(k)-cleared medical device (K760675) manufactured by Aspen Laboratories, 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 December 27, 1976. Regulation: 8.