
Bisco, Inc.
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TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P is an FDA 510(k)-cleared medical device (K024046) manufactured by Bisco, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 5, 2003. Regulation: 8.