SORING GMBH, SONOCA 300

SORING GMBH, SONOCA 300 is an FDA 510(k)-cleared medical device (K992026) manufactured by Soring GmbH Medizintechnik. 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 September 22, 1999. Regulation: 8.