
Symbiosis Corp.
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INSTRUMENT, MANUAL, GENERAL SURGICAL is an FDA 510(k)-cleared medical device (K922571) manufactured by Symbiosis Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 10, 1992. Regulation: 8.